Sequential Circulator SC-2004FC-OC

FDA 510(k) K171793 · Bio Compression Systems, Inc.

Substantially Equivalent

510(k) numberK171793

Submission

Device name
Sequential Circulator SC-2004FC-OC
Applicant
Bio Compression Systems, Inc.
Moonachie, NJ, US
Received
June 16, 2017
Decision date
August 17, 2017
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOW – Sleeve, Limb, Compressible
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5800
Specialty
Cardiovascular

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K253555Flexitouch® Plus Advanced Pneumatic Compression SystemJOW · Traditional Tactile Medical07/31/2026SE
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K250974Bio Arterial Deluxe (IC-BAP-DX)JOW · Traditional Bio Compression Systems, Inc.12/12/2025SE
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K251466VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System…JOW · Special Wellell, Inc.10/28/2025SE
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More from Manamed, LLC

510(k)DeviceDecision
K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)JOW · Traditional 09/11/2026SE
K250974Bio Arterial Deluxe (IC-BAP-DX)JOW · Traditional 12/12/2025SE
K213533Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL…IRP · Traditional 02/16/2022SE
K210417Sequential Circulators SC-1004-DL, SC-1008-DL, SC-2004-DL, SC-2008-DL, SC-4004-DL…JOW · Traditional 05/14/2021SE
K180248VascuEase IC-1200-WHJOW · Traditional 08/07/2018SE
K150953Sequential Circulator SC-2008-OC, Sequential Circulator SC-2004-OCJOW · Special 07/16/2015SE
K142640Model SC-3004-DL Sequential Circulator, Model SC-3004FC-DL Sequenstial Circulator, Model…JOW · Traditional 11/06/2014SE
K131306IC-1545-DL Multi Flo DVT Combo Intermittent Pneumatic Compression DeviceJOW · Traditional 07/22/2013SE
K131327Bioarterial Plus Arterial Blood Flow Enhancement SystemJOW · Traditional 07/18/2013SE
K1221122004-OC Massage System, 2008-OC Massage SystemIRP · Traditional 04/09/2013SE

Questions and answers

When was Sequential Circulator SC-2004FC-OC cleared by the FDA?

Sequential Circulator SC-2004FC-OC (K171793) received a 510(k) decision of Substantially Equivalent on August 17, 2017, 62 days after the submission was received.

What is the product code of K171793?

The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.