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FDA 510(k)

PULSED AND CONTINUOUS SHORTWAVE APPAR.

K-Number: K781316 · 1978-09-27

ApplicantGeneral Theraphysical, Inc.
Decision Date1978-09-27
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PULSED AND CONTINUOUS SHORTWAVE APPAR. 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 1978-09-27 under 510(k) number K781316. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSED AND CONTINUOUS SHORTWAVE APPAR.?

PULSED AND CONTINUOUS SHORTWAVE APPAR. is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is General Theraphysical, Inc.. The 510(k) number is K781316.

When did PULSED AND CONTINUOUS SHORTWAVE APPAR. receive FDA 510(k) clearance?

PULSED AND CONTINUOUS SHORTWAVE APPAR. received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781316.

Who is the listed applicant for PULSED AND CONTINUOUS SHORTWAVE APPAR.?

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 PULSED AND CONTINUOUS SHORTWAVE APPAR.?

The FDA product code for PULSED AND CONTINUOUS SHORTWAVE APPAR. is IMJ.

Related Clinical Trials

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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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 APPARATUSK781319THERAPY APPAR. 422 INTERFERENTIALK781320SHORTWAVE THERAPY APPAR. CURAMED 401

View all 7 devices →

Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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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