FDA 510(k)

SPONGE, CURITY WASHED GAUZE

K-Number: K760094 · 1976-07-16

Decision Date1976-07-16

Product CodeNAB

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SPONGE, CURITY WASHED GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Research Center. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760094. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPONGE, CURITY WASHED GAUZE?

SPONGE, CURITY WASHED GAUZE is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Kendall Research Center. The 510(k) number is K760094.

When did SPONGE, CURITY WASHED GAUZE receive FDA 510(k) clearance?

SPONGE, CURITY WASHED GAUZE received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760094.

Who is the listed applicant for SPONGE, CURITY WASHED GAUZE?

The FDA 510(k) record lists Kendall Research Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPONGE, CURITY WASHED GAUZE?

The FDA product code for SPONGE, CURITY WASHED GAUZE is NAB.

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Other records listing Kendall Research Center as applicant

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Related Devices (Code: NAB)

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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.