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FDA 510(k)

GAUZE SPONGE X-RAY DETECTABLE-

K-Number: K832172 · 1983-08-12

Decision Date1983-08-12
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GAUZE SPONGE X-RAY DETECTABLE- is the device name listed in this FDA 510(k) record. The listed applicant is Sudreca Surgical Dressings, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832172. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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