BLISTERFILM TRANSPARENT DRESSING
K-Number: K851383 · 1985-07-05
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Device Summary
Frequently Asked Questions
What is the BLISTERFILM TRANSPARENT DRESSING?
BLISTERFILM TRANSPARENT DRESSING is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K851383.
When did BLISTERFILM TRANSPARENT DRESSING receive FDA 510(k) clearance?
BLISTERFILM TRANSPARENT DRESSING received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851383.
Who is the listed applicant for BLISTERFILM TRANSPARENT DRESSING?
The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLISTERFILM TRANSPARENT DRESSING?
The FDA product code for BLISTERFILM TRANSPARENT DRESSING is NAD.
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 Chesebrough-Pond'S U.S.A. Co. 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: NAD)
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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