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FDA 510(k)

SANYO ELECTRONIC MUSCLE STIMULATORS

K-Number: K850047 · 1985-03-05

ApplicantGeneral Physiotherapy, Inc.
Decision Date1985-03-05
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SANYO ELECTRONIC MUSCLE STIMULATORS is the device name listed in this FDA 510(k) record. The listed applicant is General Physiotherapy, Inc.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K850047. 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 SANYO ELECTRONIC MUSCLE STIMULATORS?

SANYO ELECTRONIC MUSCLE STIMULATORS is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is General Physiotherapy, Inc.. The 510(k) number is K850047.

When did SANYO ELECTRONIC MUSCLE STIMULATORS receive FDA 510(k) clearance?

SANYO ELECTRONIC MUSCLE STIMULATORS received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850047.

Who is the listed applicant for SANYO ELECTRONIC MUSCLE STIMULATORS?

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

What is the FDA product code for SANYO ELECTRONIC MUSCLE STIMULATORS?

The FDA product code for SANYO ELECTRONIC MUSCLE STIMULATORS is IPF.

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Other records listing General Physiotherapy, Inc. as applicant

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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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