GAUZE SPONGE NON-STERILE
K-Number: K832174 · 1983-08-12
Advertisement
Device Summary
Frequently Asked Questions
What is the GAUZE SPONGE NON-STERILE?
GAUZE SPONGE NON-STERILE is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Sudreca Surgical Dressings, Inc.. The 510(k) number is K832174.
When did GAUZE SPONGE NON-STERILE receive FDA 510(k) clearance?
GAUZE SPONGE NON-STERILE received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832174.
Who is the listed applicant for GAUZE SPONGE NON-STERILE?
The FDA 510(k) record lists Sudreca Surgical Dressings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAUZE SPONGE NON-STERILE?
The FDA product code for GAUZE SPONGE 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 Sudreca Surgical Dressings, 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