ULCUFLEX HYDROCOLOID POWDER
K-Number: K920366 · 1992-03-26
Advertisement
Device Summary
Frequently Asked Questions
What is the ULCUFLEX HYDROCOLOID POWDER?
ULCUFLEX HYDROCOLOID POWDER is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Industrias Palex C/O Dma Med-Chem Corp.. The 510(k) number is K920366.
When did ULCUFLEX HYDROCOLOID POWDER receive FDA 510(k) clearance?
ULCUFLEX HYDROCOLOID POWDER received FDA 510(k) clearance on 1992-03-26, under 510(k) number K920366.
Who is the listed applicant for ULCUFLEX HYDROCOLOID POWDER?
The FDA 510(k) record lists Industrias Palex C/O Dma Med-Chem Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULCUFLEX HYDROCOLOID POWDER?
The FDA product code for ULCUFLEX HYDROCOLOID POWDER is KMF.
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 Industrias Palex C/O Dma Med-Chem 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: KMF)
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.
Advertisement