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FDA 510(k)

MEROCEL SOFT WOUND DRESSING

K-Number: K954919 · 1995-11-14

ApplicantMerocel Corp.
Decision Date1995-11-14
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

MEROCEL SOFT WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Merocel Corp.. It received FDA 510(k) clearance on 1995-11-14 under 510(k) number K954919. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MEROCEL SOFT WOUND DRESSING?

MEROCEL SOFT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-11-14. The listed applicant is Merocel Corp.. The 510(k) number is K954919.

When did MEROCEL SOFT WOUND DRESSING receive FDA 510(k) clearance?

MEROCEL SOFT WOUND DRESSING received FDA 510(k) clearance on 1995-11-14, under 510(k) number K954919.

Who is the listed applicant for MEROCEL SOFT WOUND DRESSING?

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

What is the FDA product code for MEROCEL SOFT WOUND DRESSING?

The FDA product code for MEROCEL SOFT WOUND DRESSING is KMF.

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Other records listing Merocel Corp. 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.

K953072MEROCEL VAGINAL PACKK953013MEROCEL REINFORCED SILICONE SHEETSK943718EPISTAT-II NASAL CATHETERK940572MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)K935658MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINTK933152MEROCEL MEROSPLINT

View all 10 devices →

Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, 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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