KOLD WRAP STERILE BURN DRESSING
K-Number: K920554 · 1993-02-19
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Device Summary
Frequently Asked Questions
What is the KOLD WRAP STERILE BURN DRESSING?
KOLD WRAP STERILE BURN DRESSING is a medical device that received FDA 510(k) clearance on 1993-02-19. The listed applicant is Kold Products. The 510(k) number is K920554.
When did KOLD WRAP STERILE BURN DRESSING receive FDA 510(k) clearance?
KOLD WRAP STERILE BURN DRESSING received FDA 510(k) clearance on 1993-02-19, under 510(k) number K920554.
Who is the listed applicant for KOLD WRAP STERILE BURN DRESSING?
The FDA 510(k) record lists Kold Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KOLD WRAP STERILE BURN DRESSING?
The FDA product code for KOLD WRAP STERILE BURN DRESSING is MGQ.
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 Kold Products 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: MGQ)
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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