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FDA 510(k)

GOOD VIBRATIONS TUBE MASSAGER

K-Number: K910519 · 1991-04-01

ApplicantDual Voltage, Inc.
Decision Date1991-04-01
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GOOD VIBRATIONS TUBE MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Dual Voltage, Inc.. It received FDA 510(k) clearance on 1991-04-01 under 510(k) number K910519. 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 GOOD VIBRATIONS TUBE MASSAGER?

GOOD VIBRATIONS TUBE MASSAGER is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Dual Voltage, Inc.. The 510(k) number is K910519.

When did GOOD VIBRATIONS TUBE MASSAGER receive FDA 510(k) clearance?

GOOD VIBRATIONS TUBE MASSAGER received FDA 510(k) clearance on 1991-04-01, under 510(k) number K910519.

Who is the listed applicant for GOOD VIBRATIONS TUBE MASSAGER?

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

What is the FDA product code for GOOD VIBRATIONS TUBE MASSAGER?

The FDA product code for GOOD VIBRATIONS TUBE MASSAGER 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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