RecallHawk

STATIM 6000B Vacuum Autoclave

Scican , Ltd.

Summary

Scican , Ltd. received 510(k) clearance for STATIM 6000B Vacuum Autoclave, a FLE device. Cleared on 2022-03-31.

Details

Source

510(k) Clearance

External ID

K214057

Action Date

2022-03-31

Status

Abbreviated

Category

device

Product Code

FLE

Product Description

STATIM 6000B Vacuum Autoclave. Product code: FLE.

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.

Scican , Ltd. has 3 FDA actions in our database, including 2 recalls and 1 clearance.

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 Scican , Ltd. have FDA actions?

Scican , Ltd. has 3 FDA actions in our database, including 2 recalls and 1 device clearance.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K214057" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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