Dermatac Drape
K-Number: K220560 · 2022-07-14
Device Summary
Frequently Asked Questions
What is the Dermatac Drape?
Dermatac Drape is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is 3M. The 510(k) number is K220560.
When did Dermatac Drape receive FDA 510(k) clearance?
Dermatac Drape received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220560.
Who is the listed applicant for Dermatac Drape?
The FDA 510(k) record lists 3M as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dermatac Drape?
The FDA product code for Dermatac Drape is OMP.
Other records listing 3M 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: OMP)
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.