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FDA 510(k)

JUHN TYM-TAP

K-Number: K790915 · 1979-06-27

ApplicantXomed, Inc.
Decision Date1979-06-27
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

JUHN TYM-TAP is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K790915. The device is classified under product code FMH. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JUHN TYM-TAP?

JUHN TYM-TAP is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Xomed, Inc.. The 510(k) number is K790915.

When did JUHN TYM-TAP receive FDA 510(k) clearance?

JUHN TYM-TAP received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790915.

Who is the listed applicant for JUHN TYM-TAP?

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

What is the FDA product code for JUHN TYM-TAP?

The FDA product code for JUHN TYM-TAP is FMH.

Other records listing Xomed, 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.

K002395MODEL 30 CLASSIC PNEUMATONOMETERK002987REDTRONIC XOMED MONOPOLAR ENERGIZED BLADEK002828XPS NITRO SYSTEMK002897TITANIUM MIDDLE EAR PROSTHESESK993653MICRO-FRANCE TROCARS AND ACCESSORIESK001148MEROGEL OTOLOGIC PACK

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Related Devices (Code: FMH)

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.

K900983TRI-TECH URINE SPECIMEN KITTri-Tech, Inc.K823763VARIOUS-SPECIMEN COLLECTORSCordis Corp.K820180CALCULI FILTER CUPOmnimedicalK812933LANCER SPECIMEN CONTAINERSherwood Medical Co.K802340SPECIMEN SETAmerican Pharmaseal Div. AhscK802002URINE SPECIMEN CONTAINER #'S 1013-1016Pollak (Intl.), Ltd.

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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