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)

TREADMILL, DIAGNOSTIC

K-Number: K760509 · 1976-08-30

ApplicantMedcraft Corp.
Decision Date1976-08-30
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREADMILL, DIAGNOSTIC is the device name listed in this FDA 510(k) record. The listed applicant is Medcraft Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760509. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREADMILL, DIAGNOSTIC?

TREADMILL, DIAGNOSTIC is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Medcraft Corp.. The 510(k) number is K760509.

When did TREADMILL, DIAGNOSTIC receive FDA 510(k) clearance?

TREADMILL, DIAGNOSTIC received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760509.

Who is the listed applicant for TREADMILL, DIAGNOSTIC?

The FDA 510(k) record lists Medcraft Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TREADMILL, DIAGNOSTIC?

The FDA product code for TREADMILL, DIAGNOSTIC is IOL.

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 Medcraft Corp. 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.

K860467ELECTROSHOCK UNIT NEUROLOGY MODEL B-25K791795COMP-ACT IVK760510MONITORING SYSTEM, REHABILITATIONK760508ACCUTAPE 24

Related Devices (Code: IOL)

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.

K950377PARKER MODEL PEParker Treadmill Co., Inc.K950376PARKER MODEL PMParker Treadmill Co., Inc.K925839TRACKMASTERJas Manufacturing Co., Inc.K930261RTM REHABILITATION TREADMILL, MODEL #945-200Biodan Medical Systems, Ltd.K904556MANSFIELD CARDIAC ASSIST MODEL 940(TM) IABBoston Scientific CorpK913518TA620 TREADMILL CONTROLLERSiemens Burdick, Inc.

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.

↑