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FDA 510(k)

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS

K-Number: K925937 · 1993-08-09

ApplicantWells Lamont Corp.
Decision Date1993-08-09
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Wells Lamont Corp.. It received FDA 510(k) clearance on 1993-08-09 under 510(k) number K925937. 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 WELLS LAMONT HANDAGES/MED WRAP DRESSINGS?

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS is a medical device that received FDA 510(k) clearance on 1993-08-09. The listed applicant is Wells Lamont Corp.. The 510(k) number is K925937.

When did WELLS LAMONT HANDAGES/MED WRAP DRESSINGS receive FDA 510(k) clearance?

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS received FDA 510(k) clearance on 1993-08-09, under 510(k) number K925937.

Who is the listed applicant for WELLS LAMONT HANDAGES/MED WRAP DRESSINGS?

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

What is the FDA product code for WELLS LAMONT HANDAGES/MED WRAP DRESSINGS?

The FDA product code for WELLS LAMONT HANDAGES/MED WRAP DRESSINGS is KMF.

Related Clinical Trials

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Other records listing Wells Lamont 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.

K944763CUT-TEC OR WELLS LAMONT POLYESTER/WIRE CUT-RESISTANT GLOVE LINER WELLS-TEC, SCEPTERK940274NYLON LINER GLOVESK922407WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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