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FDA 510(k)

ELECTRIC VIBRATOR

K-Number: K761121 · 1976-12-02

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

Device Summary

ELECTRIC VIBRATOR 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 K761121. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC VIBRATOR?

ELECTRIC VIBRATOR 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 K761121.

When did ELECTRIC VIBRATOR receive FDA 510(k) clearance?

ELECTRIC VIBRATOR received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761121.

Who is the listed applicant for ELECTRIC VIBRATOR?

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 ELECTRIC VIBRATOR?

The FDA product code for ELECTRIC VIBRATOR is IRO.

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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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