PREP-SITE PROTECTIVE DRESSING WIPE
K-Number: K811625 · 1981-07-10
Advertisement
Device Summary
Frequently Asked Questions
What is the PREP-SITE PROTECTIVE DRESSING WIPE?
PREP-SITE PROTECTIVE DRESSING WIPE is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Acme United Corp.. The 510(k) number is K811625.
When did PREP-SITE PROTECTIVE DRESSING WIPE receive FDA 510(k) clearance?
PREP-SITE PROTECTIVE DRESSING WIPE received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811625.
Who is the listed applicant for PREP-SITE PROTECTIVE DRESSING WIPE?
The FDA 510(k) record lists Acme United Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREP-SITE PROTECTIVE DRESSING WIPE?
The FDA product code for PREP-SITE PROTECTIVE DRESSING WIPE 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 Acme United 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