3M GERMICIDAL SURGICAL INCISE DRAPE
K-Number: K801550 · 1981-09-17
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Device Summary
Frequently Asked Questions
What is the 3M GERMICIDAL SURGICAL INCISE DRAPE?
3M GERMICIDAL SURGICAL INCISE DRAPE is a medical device that received FDA 510(k) clearance on 1981-09-17. The listed applicant is 3M Company. The 510(k) number is K801550.
When did 3M GERMICIDAL SURGICAL INCISE DRAPE receive FDA 510(k) clearance?
3M GERMICIDAL SURGICAL INCISE DRAPE received FDA 510(k) clearance on 1981-09-17, under 510(k) number K801550.
Who is the listed applicant for 3M GERMICIDAL SURGICAL INCISE DRAPE?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3M GERMICIDAL SURGICAL INCISE DRAPE?
The FDA product code for 3M GERMICIDAL SURGICAL INCISE DRAPE is KKX.
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 3M Company 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: KKX)
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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