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FDA 510(k)

PLAIN DRY GAUZE

K-Number: K873523 · 1987-10-09

Decision Date1987-10-09
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

PLAIN DRY GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Absorbent Cotton Co., Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873523. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAIN DRY GAUZE?

PLAIN DRY GAUZE is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Absorbent Cotton Co., Inc.. The 510(k) number is K873523.

When did PLAIN DRY GAUZE receive FDA 510(k) clearance?

PLAIN DRY GAUZE received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873523.

Who is the listed applicant for PLAIN DRY GAUZE?

The FDA 510(k) record lists Absorbent Cotton Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLAIN DRY GAUZE?

The FDA product code for PLAIN DRY GAUZE 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 Absorbent Cotton Co., 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.

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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

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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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