PELNAC Bilayer Wound Matrix
K-Number: K191992 · 2020-04-29
Device Summary
Frequently Asked Questions
What is the PELNAC Bilayer Wound Matrix?
PELNAC Bilayer Wound Matrix is a medical device that received FDA 510(k) clearance on 2020-04-29. The listed applicant is Gunze Limited. The 510(k) number is K191992.
When did PELNAC Bilayer Wound Matrix receive FDA 510(k) clearance?
PELNAC Bilayer Wound Matrix received FDA 510(k) clearance on 2020-04-29, under 510(k) number K191992.
Who is the listed applicant for PELNAC Bilayer Wound Matrix?
The FDA 510(k) record lists Gunze Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PELNAC Bilayer Wound Matrix?
The FDA product code for PELNAC Bilayer Wound Matrix is KGN.
Other records listing Gunze Limited 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: KGN)
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.