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FDA 510(k)

BARIOR

K-Number: K770213 · 1977-02-07

ApplicantTri-Med, Inc.
Decision Date1977-02-07
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARIOR is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med, Inc.. It received FDA 510(k) clearance on 1977-02-07 under 510(k) number K770213. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARIOR?

BARIOR is a medical device that received FDA 510(k) clearance on 1977-02-07. The listed applicant is Tri-Med, Inc.. The 510(k) number is K770213.

When did BARIOR receive FDA 510(k) clearance?

BARIOR received FDA 510(k) clearance on 1977-02-07, under 510(k) number K770213.

Who is the listed applicant for BARIOR?

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

What is the FDA product code for BARIOR?

The FDA product code for BARIOR is KOC.

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Other records listing Tri-Med, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K040112TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATEK030877TRIMED RADIAL BULLETK010545TBWK961863PARACENTESIS TRAYSK875224HUDSON CRANINAL BURRSK850746TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI

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Related Devices (Code: KOC)

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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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