BURN PAD, DRY, STERILE
K-Number: K781985 · 1978-12-07
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Device Summary
Frequently Asked Questions
What is the BURN PAD, DRY, STERILE?
BURN PAD, DRY, STERILE is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K781985.
When did BURN PAD, DRY, STERILE receive FDA 510(k) clearance?
BURN PAD, DRY, STERILE received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781985.
Who is the listed applicant for BURN PAD, DRY, STERILE?
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 BURN PAD, DRY, STERILE?
The FDA product code for BURN PAD, DRY, STERILE is EFQ.
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: EFQ)
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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