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FDA 510(k)

FRASTEC DRY GAUZE BANDAGE

K-Number: K871917 · 1987-06-16

Decision Date1987-06-16
Product CodeEFQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

FRASTEC DRY GAUZE BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Fraass Survival Systems, Inc.. It received FDA 510(k) clearance on 1987-06-16 under 510(k) number K871917. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the FRASTEC DRY GAUZE BANDAGE?

FRASTEC DRY GAUZE BANDAGE is a medical device that received FDA 510(k) clearance on 1987-06-16. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K871917.

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

FRASTEC DRY GAUZE BANDAGE received FDA 510(k) clearance on 1987-06-16, under 510(k) number K871917.

Who is the listed applicant for FRASTEC DRY GAUZE BANDAGE?

The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRASTEC DRY GAUZE BANDAGE?

The FDA product code for FRASTEC DRY GAUZE BANDAGE 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 Fraass Survival Systems, 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.

View all 23 devices →

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.

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