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FDA 510(k)

LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR

K-Number: K990445 · 2000-01-18

ApplicantLpg USA, Inc.
Decision Date2000-01-18
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lpg USA, Inc.. It received FDA 510(k) clearance on 2000-01-18 under 510(k) number K990445. 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 LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR?

LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR is a medical device that received FDA 510(k) clearance on 2000-01-18. The listed applicant is Lpg USA, Inc.. The 510(k) number is K990445.

When did LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR receive FDA 510(k) clearance?

LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR received FDA 510(k) clearance on 2000-01-18, under 510(k) number K990445.

Who is the listed applicant for LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR?

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

What is the FDA product code for LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR?

The FDA product code for LPG THERAPEUTIC MASSAGER, MODELS -ESI, THERAPEUTIC MASSAGER/VIBRATOR 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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