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FDA 510(k)

NAIL CLIPPERS, ONE-HANDED

K-Number: K781200 · 1978-07-31

ApplicantFred Sammons, Inc.
Decision Date1978-07-31
Product CodeILW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NAIL CLIPPERS, ONE-HANDED is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1978-07-31 under 510(k) number K781200. The device is classified under product code ILW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAIL CLIPPERS, ONE-HANDED?

NAIL CLIPPERS, ONE-HANDED is a medical device that received FDA 510(k) clearance on 1978-07-31. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K781200.

When did NAIL CLIPPERS, ONE-HANDED receive FDA 510(k) clearance?

NAIL CLIPPERS, ONE-HANDED received FDA 510(k) clearance on 1978-07-31, under 510(k) number K781200.

Who is the listed applicant for NAIL CLIPPERS, ONE-HANDED?

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

What is the FDA product code for NAIL CLIPPERS, ONE-HANDED?

The FDA product code for NAIL CLIPPERS, ONE-HANDED is ILW.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: ILW)

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.

K823632LONG HANDLED FOLDING HAIRBRUSHFred Sammons, Inc.K810457GROOMING ADAPTORSFred Sammons, Inc.K781197STICK, UTILITYFred Sammons, Inc.K761123ELECTRIC RAZOR HOLDERFred Sammons, Inc.K760293MIRROR, EXTEND-A-, BK-6235Fred Sammons, Inc.K760289BRUSH, DISPOSA-A (HANDLE, REFILL PKG)Fred Sammons, Inc.

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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