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FDA 510(k)

PULSOR, THERAPEUTIC VIBRATOR

K-Number: K874716 · 1988-02-11

ApplicantGmg Enterprises, Inc.
Decision Date1988-02-11
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PULSOR, THERAPEUTIC VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Gmg Enterprises, Inc.. It received FDA 510(k) clearance on 1988-02-11 under 510(k) number K874716. 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 PULSOR, THERAPEUTIC VIBRATOR?

PULSOR, THERAPEUTIC VIBRATOR is a medical device that received FDA 510(k) clearance on 1988-02-11. The listed applicant is Gmg Enterprises, Inc.. The 510(k) number is K874716.

When did PULSOR, THERAPEUTIC VIBRATOR receive FDA 510(k) clearance?

PULSOR, THERAPEUTIC VIBRATOR received FDA 510(k) clearance on 1988-02-11, under 510(k) number K874716.

Who is the listed applicant for PULSOR, THERAPEUTIC VIBRATOR?

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

What is the FDA product code for PULSOR, THERAPEUTIC VIBRATOR?

The FDA product code for PULSOR, THERAPEUTIC 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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