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FDA 510(k)

BARIKARE PLUS

K-Number: K945664 · 1995-02-16

ApplicantKinetic Concepts, Inc.
Decision Date1995-02-16
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARIKARE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1995-02-16 under 510(k) number K945664. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARIKARE PLUS?

BARIKARE PLUS is a medical device that received FDA 510(k) clearance on 1995-02-16. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K945664.

When did BARIKARE PLUS receive FDA 510(k) clearance?

BARIKARE PLUS received FDA 510(k) clearance on 1995-02-16, under 510(k) number K945664.

Who is the listed applicant for BARIKARE PLUS?

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

What is the FDA product code for BARIKARE PLUS?

The FDA product code for BARIKARE PLUS is FNL.

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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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