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FDA 510(k)

THERAPY UNIT & ELECTRODIAG.

K-Number: K781314 · 1978-10-03

ApplicantGeneral Theraphysical, Inc.
Decision Date1978-10-03
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THERAPY UNIT & ELECTRODIAG. is the device name listed in this FDA 510(k) record. The listed applicant is General Theraphysical, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781314. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERAPY UNIT & ELECTRODIAG.?

THERAPY UNIT & ELECTRODIAG. is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is General Theraphysical, Inc.. The 510(k) number is K781314.

When did THERAPY UNIT & ELECTRODIAG. receive FDA 510(k) clearance?

THERAPY UNIT & ELECTRODIAG. received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781314.

Who is the listed applicant for THERAPY UNIT & ELECTRODIAG.?

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

What is the FDA product code for THERAPY UNIT & ELECTRODIAG.?

The FDA product code for THERAPY UNIT & ELECTRODIAG. is GXY.

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Other records listing General Theraphysical, Inc. as applicant

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.

K781317ULTRASONIC THERAPY APPARATUS, 407K781315MUSCLE STIMULATION APPARATUSK781318DYNATRON 406 ELECTROTHERAPY APPARATUSK781319THERAPY APPAR. 422 INTERFERENTIALK781320SHORTWAVE THERAPY APPAR. CURAMED 401K781316PULSED AND CONTINUOUS SHORTWAVE APPAR.

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Related Devices (Code: GXY)

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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