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FDA 510(k)

CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM

K-Number: K935948 · 1994-03-01

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1994-03-01
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM 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 1994-03-01 under 510(k) number K935948. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM?

CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K935948.

When did CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM receive FDA 510(k) clearance?

CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM received FDA 510(k) clearance on 1994-03-01, under 510(k) number K935948.

Who is the listed applicant for CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM?

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 TWO PIECE ABSORBENT DRESSING SYSTEM?

The FDA product code for CONVATEC TWO PIECE ABSORBENT DRESSING SYSTEM is KGX.

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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: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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