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FDA 510(k)

DISCIPLINE II RTD

K-Number: K871557 · 1987-08-26

ApplicantPhysio Systems, Inc.
Decision Date1987-08-26
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DISCIPLINE II RTD 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 1987-08-26 under 510(k) number K871557. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCIPLINE II RTD?

DISCIPLINE II RTD is a medical device that received FDA 510(k) clearance on 1987-08-26. The listed applicant is Physio Systems, Inc.. The 510(k) number is K871557.

When did DISCIPLINE II RTD receive FDA 510(k) clearance?

DISCIPLINE II RTD received FDA 510(k) clearance on 1987-08-26, under 510(k) number K871557.

Who is the listed applicant for DISCIPLINE II RTD?

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 II RTD?

The FDA product code for DISCIPLINE II RTD is IKK.

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)K870872DISCIPLINE I

Related Devices (Code: IKK)

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.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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