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FDA 510(k)

GIBSON ID-M. CAT.

K-Number: K955826 · 1996-02-29

ApplicantGibson Laboratories, Inc.
Decision Date1996-02-29
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GIBSON ID-M. CAT. is the device name listed in this FDA 510(k) record. The listed applicant is Gibson Laboratories, Inc.. It received FDA 510(k) clearance on 1996-02-29 under 510(k) number K955826. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIBSON ID-M. CAT.?

GIBSON ID-M. CAT. is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Gibson Laboratories, Inc.. The 510(k) number is K955826.

When did GIBSON ID-M. CAT. receive FDA 510(k) clearance?

GIBSON ID-M. CAT. received FDA 510(k) clearance on 1996-02-29, under 510(k) number K955826.

Who is the listed applicant for GIBSON ID-M. CAT.?

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

What is the FDA product code for GIBSON ID-M. CAT.?

The FDA product code for GIBSON ID-M. CAT. is JTO.

Related Clinical Trials

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.

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Other records listing Gibson Laboratories, 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.

K953247GIBSON ID A.E. TESTK905120SAF FIXATIVEK904773P AND T MEDIUM

Related Devices (Code: JTO)

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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, Inc.

Official Source

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

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