RecallHawk

VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Ma

Acist Medical Systems, Inc.

Summary

Acist Medical Systems, Inc. received 510(k) clearance for VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804), a DXT device. Cleared on 2026-05-13.

Details

Source

510(k) Clearance

External ID

K252638

Action Date

2026-05-13

Status

Traditional

Category

device

Product Code

DXT

Product Description

VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804). Product code: DXT.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Acist Medical Systems, Inc. has received 3 total clearances in our database.

Acist Medical Systems, Inc. has 3 FDA actions in our database, including 3 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Acist Medical Systems, Inc. have FDA actions?

Acist Medical Systems, Inc. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K252638" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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