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FDA 510(k)

GRX FOAM DRESSING

K-Number: K945224 · 1995-04-03

ApplicantGeritrex Corp.
Decision Date1995-04-03
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRX FOAM DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Geritrex Corp.. It received FDA 510(k) clearance on 1995-04-03 under 510(k) number K945224. 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 GRX FOAM DRESSING?

GRX FOAM DRESSING is a medical device that received FDA 510(k) clearance on 1995-04-03. The listed applicant is Geritrex Corp.. The 510(k) number is K945224.

When did GRX FOAM DRESSING receive FDA 510(k) clearance?

GRX FOAM DRESSING received FDA 510(k) clearance on 1995-04-03, under 510(k) number K945224.

Who is the listed applicant for GRX FOAM DRESSING?

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

What is the FDA product code for GRX FOAM DRESSING?

The FDA product code for GRX FOAM DRESSING is KMF.

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Other records listing Geritrex 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.

K931509GERITREX STERILE SALINE SOLUTION FOR IRRIGATIONK931511GERITREX STERILE WATER FOR IRRIGATIONK931510GERITREX STERILE SALINE WET DRESSING

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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