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FDA 510(k)

BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE)

K-Number: K870185 · 1987-02-06

ApplicantFraass Survival Systems, Inc.
Decision Date1987-02-06
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE) 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 1987-02-06 under 510(k) number K870185. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE)?

BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE) is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K870185.

When did BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE) receive FDA 510(k) clearance?

BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE) received FDA 510(k) clearance on 1987-02-06, under 510(k) number K870185.

Who is the listed applicant for BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE)?

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 BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE)?

The FDA product code for BANDAGE, GAUZE (NONABSOR. GAUZE FOR EXTERNAL USE) is NAD.

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Other records listing Fraass Survival Systems, Inc. as applicant

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Related Devices (Code: NAD)

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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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