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FDA 510(k)

MEROCEL INSTRUMENT WIPE

K-Number: K791736 · 1979-09-19

ApplicantXomed, Inc.
Decision Date1979-09-19
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEROCEL INSTRUMENT WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-09-19 under 510(k) number K791736. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEROCEL INSTRUMENT WIPE?

MEROCEL INSTRUMENT WIPE is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Xomed, Inc.. The 510(k) number is K791736.

When did MEROCEL INSTRUMENT WIPE receive FDA 510(k) clearance?

MEROCEL INSTRUMENT WIPE received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791736.

Who is the listed applicant for MEROCEL INSTRUMENT WIPE?

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 MEROCEL INSTRUMENT WIPE?

The FDA product code for MEROCEL INSTRUMENT WIPE is GEC.

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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: GEC)

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.

K971473IVALON INSTRUMENT WIPE, IVALON KNIFE CLEANING BLOCKM-Pact Worldwide Management Corp.K960621EXPANDACELL INSTRUMENT WIPEShippert Medical Technologies Corp.K900691BIODYNE INSTRUMENT WIPESBio-Dyne, Inc.K896085SURGI-BRUSHSparta Surgical Corp.K875033STERILE SCRUBBY SCRUB BRUSHMedsurg Industries, Inc.K875129STERI-CLENSAbsorbent Cotton Co., 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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