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FDA 510(k)

THERAPY APPAR. 422 INTERFERENTIAL

K-Number: K781319 · 1978-10-03

ApplicantGeneral Theraphysical, Inc.
Decision Date1978-10-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERAPY APPAR. 422 INTERFERENTIAL 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 K781319. 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 THERAPY APPAR. 422 INTERFERENTIAL?

THERAPY APPAR. 422 INTERFERENTIAL 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 K781319.

When did THERAPY APPAR. 422 INTERFERENTIAL receive FDA 510(k) clearance?

THERAPY APPAR. 422 INTERFERENTIAL received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781319.

Who is the listed applicant for THERAPY APPAR. 422 INTERFERENTIAL?

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 APPAR. 422 INTERFERENTIAL?

The FDA product code for THERAPY APPAR. 422 INTERFERENTIAL is IPF.

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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 APPARATUSK781314THERAPY UNIT & ELECTRODIAG.K781318DYNATRON 406 ELECTROTHERAPY APPARATUSK781320SHORTWAVE THERAPY APPAR. CURAMED 401K781316PULSED AND CONTINUOUS SHORTWAVE APPAR.

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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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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