GAUZE SWABS, NON-STERILE
K-Number: K885142 · 1989-01-24
Advertisement
Device Summary
Frequently Asked Questions
What is the GAUZE SWABS, NON-STERILE?
GAUZE SWABS, NON-STERILE is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K885142.
When did GAUZE SWABS, NON-STERILE receive FDA 510(k) clearance?
GAUZE SWABS, NON-STERILE received FDA 510(k) clearance on 1989-01-24, under 510(k) number K885142.
Who is the listed applicant for GAUZE SWABS, NON-STERILE?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE SWABS, NON-STERILE?
The FDA product code for GAUZE SWABS, NON-STERILE is EFQ.
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 Smith & Nephew, 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: EFQ)
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