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FDA 510(k)

MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)

K-Number: K940572 · 1994-06-07

ApplicantMerocel Corp.
Decision Date1994-06-07
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) is the device name listed in this FDA 510(k) record. The listed applicant is Merocel Corp.. It received FDA 510(k) clearance on 1994-06-07 under 510(k) number K940572. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)?

MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Merocel Corp.. The 510(k) number is K940572.

When did MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) receive FDA 510(k) clearance?

MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) received FDA 510(k) clearance on 1994-06-07, under 510(k) number K940572.

Who is the listed applicant for MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)?

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(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)?

The FDA product code for MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) 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.

K954919MEROCEL SOFT WOUND DRESSINGK953072MEROCEL VAGINAL PACKK953013MEROCEL REINFORCED SILICONE SHEETSK943718EPISTAT-II NASAL CATHETERK935658MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINTK933152MEROCEL MEROSPLINT

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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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