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)

PARKER MODEL PE

K-Number: K950377 · 1995-09-06

ApplicantParker Treadmill Co., Inc.
Decision Date1995-09-06
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PARKER MODEL PE is the device name listed in this FDA 510(k) record. The listed applicant is Parker Treadmill Co., Inc.. It received FDA 510(k) clearance on 1995-09-06 under 510(k) number K950377. 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 PARKER MODEL PE?

PARKER MODEL PE is a medical device that received FDA 510(k) clearance on 1995-09-06. The listed applicant is Parker Treadmill Co., Inc.. The 510(k) number is K950377.

When did PARKER MODEL PE receive FDA 510(k) clearance?

PARKER MODEL PE received FDA 510(k) clearance on 1995-09-06, under 510(k) number K950377.

Who is the listed applicant for PARKER MODEL PE?

The FDA 510(k) record lists Parker Treadmill Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARKER MODEL PE?

The FDA product code for PARKER MODEL PE 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 Parker Treadmill Co., 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.

K950376PARKER MODEL PM

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.

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.K910867T600 TREADMILLSiemens 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.

↑