GAUZE SPONGE X-RAY DETECTABLE-
K-Number: K832172 · 1983-08-12
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Device Summary
Frequently Asked Questions
What is the GAUZE SPONGE X-RAY DETECTABLE-?
GAUZE SPONGE X-RAY DETECTABLE- 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 K832172.
When did GAUZE SPONGE X-RAY DETECTABLE- receive FDA 510(k) clearance?
GAUZE SPONGE X-RAY DETECTABLE- received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832172.
Who is the listed applicant for GAUZE SPONGE X-RAY DETECTABLE-?
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 X-RAY DETECTABLE-?
The FDA product code for GAUZE SPONGE X-RAY DETECTABLE- is GDY.
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: GDY)
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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