DERMASSIST PETROLATUM GAUZE,USP
K-Number: K936230 · 1994-03-03
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Device Summary
Frequently Asked Questions
What is the DERMASSIST PETROLATUM GAUZE,USP?
DERMASSIST PETROLATUM GAUZE,USP is a medical device that received FDA 510(k) clearance on 1994-03-03. The listed applicant is Wilshire Medical Products. The 510(k) number is K936230.
When did DERMASSIST PETROLATUM GAUZE,USP receive FDA 510(k) clearance?
DERMASSIST PETROLATUM GAUZE,USP received FDA 510(k) clearance on 1994-03-03, under 510(k) number K936230.
Who is the listed applicant for DERMASSIST PETROLATUM GAUZE,USP?
The FDA 510(k) record lists Wilshire Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DERMASSIST PETROLATUM GAUZE,USP?
The FDA product code for DERMASSIST PETROLATUM GAUZE,USP is FRO. This falls under the Anesthesiology category.
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 Wilshire Medical 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: FRO)
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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