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FDA 510(k)

HAND TOWEL

K-Number: K791926 · 1979-10-17

ApplicantProcter & Gamble Mfg. Co.
Decision Date1979-10-17
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HAND TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1979-10-17 under 510(k) number K791926. 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 HAND TOWEL?

HAND TOWEL is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K791926.

When did HAND TOWEL receive FDA 510(k) clearance?

HAND TOWEL received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791926.

Who is the listed applicant for HAND TOWEL?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAND TOWEL?

The FDA product code for HAND TOWEL is NAB.

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Other records listing Procter & Gamble Mfg. Co. 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.

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