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FDA 510(k)

PM 2000 AUTOMATIC PATIENT CHAIR

K-Number: K781597 · 1978-09-27

ApplicantTime Motion System Co.
Decision Date1978-09-27
Product CodeFFG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PM 2000 AUTOMATIC PATIENT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Time Motion System Co.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781597. The device is classified under product code FFG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PM 2000 AUTOMATIC PATIENT CHAIR?

PM 2000 AUTOMATIC PATIENT CHAIR is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Time Motion System Co.. The 510(k) number is K781597.

When did PM 2000 AUTOMATIC PATIENT CHAIR receive FDA 510(k) clearance?

PM 2000 AUTOMATIC PATIENT CHAIR received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781597.

Who is the listed applicant for PM 2000 AUTOMATIC PATIENT CHAIR?

The FDA 510(k) record lists Time Motion System Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PM 2000 AUTOMATIC PATIENT CHAIR?

The FDA product code for PM 2000 AUTOMATIC PATIENT CHAIR is FFG.

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 Time Motion System Co. 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.

K820789CANCAN 2002 DENTAL PATIENT CHAIR

Related Devices (Code: FFG)

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.

K893827PEAK FLOW RATE METERLaytech Medical Co.K883274SURGITEK (R) UROFLOW SYSTEMMedical Engineering Corp.K850169ERIS URO-DIAGNOSTIC SYSTEMEris Medical TechnologyK8443381URO-LOG HOME DIAGNOSTIC PACKEpcom Medical Systems, Inc.K843442URINARY DRAINAGE CONTAINER 2013 WITHVital Metrics, Inc.K843441URINARY DRAINAGE CONTAINER 2012-WITHVital Metrics, 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.

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