DERMASORB WOUND CONTACT LAYER DRESSING
K-Number: K903645 · 1990-11-21
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Device Summary
Frequently Asked Questions
What is the DERMASORB WOUND CONTACT LAYER DRESSING?
DERMASORB WOUND CONTACT LAYER DRESSING is a medical device that received FDA 510(k) clearance on 1990-11-21. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K903645.
When did DERMASORB WOUND CONTACT LAYER DRESSING receive FDA 510(k) clearance?
DERMASORB WOUND CONTACT LAYER DRESSING received FDA 510(k) clearance on 1990-11-21, under 510(k) number K903645.
Who is the listed applicant for DERMASORB WOUND CONTACT LAYER 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 DERMASORB WOUND CONTACT LAYER DRESSING?
The FDA product code for DERMASORB WOUND CONTACT LAYER DRESSING is KOZ.
Related Clinical Trials
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.
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.
Related Devices (Code: KOZ)
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.
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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