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FDA 510(k)

SHORTWAVE THERAPY APPAR. CURAMED 401

K-Number: K781320 · 1978-09-27

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

Device Summary

SHORTWAVE THERAPY APPAR. CURAMED 401 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 K781320. 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 SHORTWAVE THERAPY APPAR. CURAMED 401?

SHORTWAVE THERAPY APPAR. CURAMED 401 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 K781320.

When did SHORTWAVE THERAPY APPAR. CURAMED 401 receive FDA 510(k) clearance?

SHORTWAVE THERAPY APPAR. CURAMED 401 received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781320.

Who is the listed applicant for SHORTWAVE THERAPY APPAR. CURAMED 401?

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 SHORTWAVE THERAPY APPAR. CURAMED 401?

The FDA product code for SHORTWAVE THERAPY APPAR. CURAMED 401 is IMJ.

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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 INTERFERENTIALK781316PULSED AND CONTINUOUS SHORTWAVE APPAR.

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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