CARRINGTON WOUND DRESSING
K-Number: K902345 · 1990-06-07
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Device Summary
Frequently Asked Questions
What is the CARRINGTON WOUND DRESSING?
CARRINGTON WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1990-06-07. The listed applicant is Carrington Laboratories, Inc.. The 510(k) number is K902345.
When did CARRINGTON WOUND DRESSING receive FDA 510(k) clearance?
CARRINGTON WOUND DRESSING received FDA 510(k) clearance on 1990-06-07, under 510(k) number K902345.
Who is the listed applicant for CARRINGTON WOUND DRESSING?
The FDA 510(k) record lists Carrington Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARRINGTON WOUND DRESSING?
The FDA product code for CARRINGTON WOUND DRESSING is FRO. This falls under the Anesthesiology category.
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 Carrington Laboratories, Inc. 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: FRO)
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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