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FDA 510(k)

FINGER EXERCISE BOARD

K-Number: K772404 · 1978-02-13

ApplicantFred Sammons, Inc.
Decision Date1978-02-13
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FINGER EXERCISE BOARD 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 1978-02-13 under 510(k) number K772404. 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 FINGER EXERCISE BOARD?

FINGER EXERCISE BOARD is a medical device that received FDA 510(k) clearance on 1978-02-13. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K772404.

When did FINGER EXERCISE BOARD receive FDA 510(k) clearance?

FINGER EXERCISE BOARD received FDA 510(k) clearance on 1978-02-13, under 510(k) number K772404.

Who is the listed applicant for FINGER EXERCISE BOARD?

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 FINGER EXERCISE BOARD?

The FDA product code for FINGER EXERCISE BOARD is ION.

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Other records listing Fred Sammons, Inc. as applicant

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.

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Related Devices (Code: 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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