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FDA 510(k)

CONVATEC NON-ADHESIVE DRESSING

K-Number: K972062 · 1997-08-14

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1997-08-14
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONVATEC NON-ADHESIVE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1997-08-14 under 510(k) number K972062. 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 CONVATEC NON-ADHESIVE DRESSING?

CONVATEC NON-ADHESIVE DRESSING is a medical device that received FDA 510(k) clearance on 1997-08-14. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K972062.

When did CONVATEC NON-ADHESIVE DRESSING receive FDA 510(k) clearance?

CONVATEC NON-ADHESIVE DRESSING received FDA 510(k) clearance on 1997-08-14, under 510(k) number K972062.

Who is the listed applicant for CONVATEC NON-ADHESIVE DRESSING?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVATEC NON-ADHESIVE DRESSING?

The FDA product code for CONVATEC NON-ADHESIVE DRESSING is KMF.

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Other records listing Convatec, A Division of E.R. Squibb & Sons 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.

K013814ABSORBENT ANTIMICROBIAL WOUND DRESSINGK990964SIGNADRESS DUODERM DRESSINGK984388HA ABSORBENT WOUND DRESSINGK980720NONWOVEN PADK980382NON-WOVEN COMPRESSK974823NONWOVEN DRESSING

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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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