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FDA 510(k)

VIBRATOR

K-Number: K810446 · 1981-03-04

ApplicantFred Sammons, Inc.
Decision Date1981-03-04
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

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 1981-03-04 under 510(k) number K810446. 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 VIBRATOR?

VIBRATOR is a medical device that received FDA 510(k) clearance on 1981-03-04. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K810446.

When did VIBRATOR receive FDA 510(k) clearance?

VIBRATOR received FDA 510(k) clearance on 1981-03-04, under 510(k) number K810446.

Who is the listed applicant for 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 VIBRATOR?

The FDA product code for VIBRATOR is IRO.

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Other records listing Fred Sammons, Inc. as applicant

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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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