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FDA 510(k)

TISSURE RETRACTORS

K-Number: K791122 · 1979-07-10

ApplicantXomed, Inc.
Decision Date1979-07-10
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TISSURE RETRACTORS is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-07-10 under 510(k) number K791122. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSURE RETRACTORS?

TISSURE RETRACTORS is a medical device that received FDA 510(k) clearance on 1979-07-10. The listed applicant is Xomed, Inc.. The 510(k) number is K791122.

When did TISSURE RETRACTORS receive FDA 510(k) clearance?

TISSURE RETRACTORS received FDA 510(k) clearance on 1979-07-10, under 510(k) number K791122.

Who is the listed applicant for TISSURE RETRACTORS?

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 TISSURE RETRACTORS?

The FDA product code for TISSURE RETRACTORS is GAD.

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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: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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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