STERIGAUZE WET DRESSING
K-Number: K952420 · 1995-07-12
Advertisement
Device Summary
Frequently Asked Questions
What is the STERIGAUZE WET DRESSING?
STERIGAUZE WET DRESSING is a medical device that received FDA 510(k) clearance on 1995-07-12. The listed applicant is Acacia Laboratories, Inc.. The 510(k) number is K952420.
When did STERIGAUZE WET DRESSING receive FDA 510(k) clearance?
STERIGAUZE WET DRESSING received FDA 510(k) clearance on 1995-07-12, under 510(k) number K952420.
Who is the listed applicant for STERIGAUZE WET DRESSING?
The FDA 510(k) record lists Acacia Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERIGAUZE WET DRESSING?
The FDA product code for STERIGAUZE WET DRESSING 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 Acacia Laboratories, Inc. 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