RecallHawk

Summary

CIVCO Medical Instruments Co., Inc. received 510(k) clearance for CIV-Clear cover, a ITX device. Cleared on 2021-09-13.

Details

Source

510(k) Clearance

External ID

K211270

Action Date

2021-09-13

Status

Traditional

Category

device

Product Code

ITX

Product Description

CIV-Clear cover. Product code: ITX.

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. CIVCO Medical Instruments Co., Inc. has received 3 total clearances in our database.

CIVCO Medical Instruments Co., Inc. has 16 FDA actions in our database, including 13 recalls and 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 CIVCO Medical Instruments Co., Inc. have FDA actions?

CIVCO Medical Instruments Co., Inc. has 16 FDA actions in our database, including 13 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K211270" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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