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FDA 510(k)

STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES

K-Number: K003857 · 2001-10-18

ApplicantSterilmed, Inc.
Decision Date2001-10-18
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2001-10-18 under 510(k) number K003857. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES?

STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES is a medical device that received FDA 510(k) clearance on 2001-10-18. The listed applicant is Sterilmed, Inc.. The 510(k) number is K003857.

When did STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES receive FDA 510(k) clearance?

STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES received FDA 510(k) clearance on 2001-10-18, under 510(k) number K003857.

Who is the listed applicant for STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES?

The FDA 510(k) record lists Sterilmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES?

The FDA product code for STERILMED INTERMITTENT COMPRESSION SYSTEM, GARMENT MODELS 400 SERIES is JOW.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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