BARRIER BURN SHEET
K-Number: K821835 · 1982-07-02
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Device Summary
Frequently Asked Questions
What is the BARRIER BURN SHEET?
BARRIER BURN SHEET is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Uhi Corp.. The 510(k) number is K821835.
When did BARRIER BURN SHEET receive FDA 510(k) clearance?
BARRIER BURN SHEET received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821835.
Who is the listed applicant for BARRIER BURN SHEET?
The FDA 510(k) record lists Uhi Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARRIER BURN SHEET?
The FDA product code for BARRIER BURN SHEET is KME.
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 Uhi Corp. 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: KME)
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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