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FDA 510(k)

DISCIPLINE I

K-Number: K870872 · 1987-03-23

ApplicantPhysio Systems, Inc.
Decision Date1987-03-23
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DISCIPLINE I is the device name listed in this FDA 510(k) record. The listed applicant is Physio Systems, Inc.. It received FDA 510(k) clearance on 1987-03-23 under 510(k) number K870872. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCIPLINE I?

DISCIPLINE I is a medical device that received FDA 510(k) clearance on 1987-03-23. The listed applicant is Physio Systems, Inc.. The 510(k) number is K870872.

When did DISCIPLINE I receive FDA 510(k) clearance?

DISCIPLINE I received FDA 510(k) clearance on 1987-03-23, under 510(k) number K870872.

Who is the listed applicant for DISCIPLINE I?

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

What is the FDA product code for DISCIPLINE I?

The FDA product code for DISCIPLINE I is ISD.

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 Physio Systems, 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.

K910712VILLAN (VIDEO LIFT LINK ANALYSIS)K871557DISCIPLINE II RTD

Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, 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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