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FDA 510(k)

HAND SCREW CLAMP

K-Number: K761118 · 1976-12-02

ApplicantFred Sammons, Inc.
Decision Date1976-12-02
Product CodeIOD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAND SCREW CLAMP 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 1976-12-02 under 510(k) number K761118. The device is classified under product code IOD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND SCREW CLAMP?

HAND SCREW CLAMP is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K761118.

When did HAND SCREW CLAMP receive FDA 510(k) clearance?

HAND SCREW CLAMP received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761118.

Who is the listed applicant for HAND SCREW CLAMP?

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 HAND SCREW CLAMP?

The FDA product code for HAND SCREW CLAMP is IOD.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: IOD)

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.

K831544DELUXE TRACTION EXERCISE GLOVE BK5035Fred Sammons, Inc.K823648SURGICAL TUBINGFred Sammons, Inc.K823822ANKLE WEIGHTSDanek Medical, Inc.K823600SOLID WOOD CONEFred Sammons, Inc.K813632COLOR CODED WEIGHT CUFFSFred Sammons, Inc.K812319THERAPY BENCHKaye Products, 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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