Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL, SC-4008-DL
Summary
Bio Compression Systems, Inc. received 510(k) clearance for Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL, SC-4008-DL, a IRP device. Cleared on 2022-02-16.
Details
Source
510(k) Clearance
External ID
K213533
Action Date
2022-02-16
Status
Traditional
Category
device
Product Code
IRP
Product Description
Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL, SC-4008-DL. Product code: IRP.
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. Bio Compression Systems, Inc. has received 2 total clearances in our database.
Bio Compression Systems, Inc. has 2 FDA actions in our database, including 2 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 Bio Compression Systems, Inc. have FDA actions?
Bio Compression Systems, Inc. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K213533" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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