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FDA 510(k)

STIMULATOR, ELECTRICAL MUSCLE (#MD-4)

K-Number: K760547 · 1977-02-17

ApplicantR. A. Fischer Co. Corp.
Decision Date1977-02-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, ELECTRICAL MUSCLE (#MD-4) is the device name listed in this FDA 510(k) record. The listed applicant is R. A. Fischer Co. Corp.. It received FDA 510(k) clearance on 1977-02-17 under 510(k) number K760547. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, ELECTRICAL MUSCLE (#MD-4)?

STIMULATOR, ELECTRICAL MUSCLE (#MD-4) is a medical device that received FDA 510(k) clearance on 1977-02-17. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K760547.

When did STIMULATOR, ELECTRICAL MUSCLE (#MD-4) receive FDA 510(k) clearance?

STIMULATOR, ELECTRICAL MUSCLE (#MD-4) received FDA 510(k) clearance on 1977-02-17, under 510(k) number K760547.

Who is the listed applicant for STIMULATOR, ELECTRICAL MUSCLE (#MD-4)?

The FDA 510(k) record lists R. A. Fischer Co. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMULATOR, ELECTRICAL MUSCLE (#MD-4)?

The FDA product code for STIMULATOR, ELECTRICAL MUSCLE (#MD-4) is IPF.

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Other records listing R. A. Fischer Co. Corp. as applicant

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K964208MD-1A GALVANIC UNITK954031COMPU-BLEND EPILATORK895365MD-2 IONTOPHORESIS UNITK893389MODEL SE-5 EPILATORK884079MODEL CBX EPILATORK871372CB-7 ELECTRONIC EPILATOR

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Related Devices (Code: IPF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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