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FDA 510(k)

SPIN-A-PULL

K-Number: K761120 · 1976-12-02

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

Device Summary

SPIN-A-PULL 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 K761120. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIN-A-PULL?

SPIN-A-PULL 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 K761120.

When did SPIN-A-PULL receive FDA 510(k) clearance?

SPIN-A-PULL received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761120.

Who is the listed applicant for SPIN-A-PULL?

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 SPIN-A-PULL?

The FDA product code for SPIN-A-PULL is ION.

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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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