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FDA 510(k)

HANDY VIBRO BELT

K-Number: K925036 · 1993-06-29

ApplicantCosmesearch, Inc.
Decision Date1993-06-29
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HANDY VIBRO BELT is the device name listed in this FDA 510(k) record. The listed applicant is Cosmesearch, Inc.. It received FDA 510(k) clearance on 1993-06-29 under 510(k) number K925036. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANDY VIBRO BELT?

HANDY VIBRO BELT is a medical device that received FDA 510(k) clearance on 1993-06-29. The listed applicant is Cosmesearch, Inc.. The 510(k) number is K925036.

When did HANDY VIBRO BELT receive FDA 510(k) clearance?

HANDY VIBRO BELT received FDA 510(k) clearance on 1993-06-29, under 510(k) number K925036.

Who is the listed applicant for HANDY VIBRO BELT?

The FDA 510(k) record lists Cosmesearch, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HANDY VIBRO BELT?

The FDA product code for HANDY VIBRO BELT is ISA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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