Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ULTRASONIC THERAPY APPARATUS, 407

K-Number: K781317 · 1978-10-03

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

Device Summary

ULTRASONIC THERAPY APPARATUS, 407 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 K781317. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC THERAPY APPARATUS, 407?

ULTRASONIC THERAPY APPARATUS, 407 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 K781317.

When did ULTRASONIC THERAPY APPARATUS, 407 receive FDA 510(k) clearance?

ULTRASONIC THERAPY APPARATUS, 407 received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781317.

Who is the listed applicant for ULTRASONIC THERAPY APPARATUS, 407?

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 ULTRASONIC THERAPY APPARATUS, 407?

The FDA product code for ULTRASONIC THERAPY APPARATUS, 407 is IMI.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K781315MUSCLE STIMULATION APPARATUSK781314THERAPY UNIT & ELECTRODIAG.K781318DYNATRON 406 ELECTROTHERAPY APPARATUSK781319THERAPY APPAR. 422 INTERFERENTIALK781320SHORTWAVE THERAPY APPAR. CURAMED 401K781316PULSED AND CONTINUOUS SHORTWAVE APPAR.

View all 7 devices →

Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , Ltd.

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.

↑