FRASTEC DRY BURN DRESSING
K-Number: K871916 · 1987-06-16
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Device Summary
Frequently Asked Questions
What is the FRASTEC DRY BURN DRESSING?
FRASTEC DRY BURN DRESSING is a medical device that received FDA 510(k) clearance on 1987-06-16. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K871916.
When did FRASTEC DRY BURN DRESSING receive FDA 510(k) clearance?
FRASTEC DRY BURN DRESSING received FDA 510(k) clearance on 1987-06-16, under 510(k) number K871916.
Who is the listed applicant for FRASTEC DRY BURN DRESSING?
The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FRASTEC DRY BURN DRESSING?
The FDA product code for FRASTEC DRY BURN DRESSING 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 Fraass Survival Systems, 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: 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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