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FDA 510(k)

MICRO & MINI-MICRO ALLIGATOR FORCEPS

K-Number: K822369 · 1982-09-09

ApplicantTreace Medical, Inc.
Decision Date1982-09-09
Product CodeKAE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICRO & MINI-MICRO ALLIGATOR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1982-09-09 under 510(k) number K822369. The device is classified under product code KAE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO & MINI-MICRO ALLIGATOR FORCEPS?

MICRO & MINI-MICRO ALLIGATOR FORCEPS is a medical device that received FDA 510(k) clearance on 1982-09-09. The listed applicant is Treace Medical, Inc.. The 510(k) number is K822369.

When did MICRO & MINI-MICRO ALLIGATOR FORCEPS receive FDA 510(k) clearance?

MICRO & MINI-MICRO ALLIGATOR FORCEPS received FDA 510(k) clearance on 1982-09-09, under 510(k) number K822369.

Who is the listed applicant for MICRO & MINI-MICRO ALLIGATOR FORCEPS?

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

What is the FDA product code for MICRO & MINI-MICRO ALLIGATOR FORCEPS?

The FDA product code for MICRO & MINI-MICRO ALLIGATOR FORCEPS is KAE.

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 Treace Medical, 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.

K883727BUCKET PROSTHESIS PORPK882349MALLET, SURGICALK874779BIPOLATOR 50K873154TREACE MAGNUM OTO-TOOL SYSTEMK872000EYE GARDK870765CANNULATED INSTRUMENT CLEANERS

View all 80 devices →

Related Devices (Code: KAE)

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.

K853708LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLEDowns Surgical , Ltd.K85179441-180 TO 41-246 VARIOUS NASAL FORCEPSArtiberiaK85177519-790 TO 19-1042 DRESSING/SPONGE FORCEPSArtiberiaK85179541-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPSArtiberiaK833608GOLD ALLIGATOR FORCEPSMicrotek Medical, Inc.K833605CUPPED FORCEPSMicrotek Medical, Inc.

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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