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FDA 510(k)

TELEVISION CONTROL OPTION 1219

K-Number: K850313 · 1985-04-25

ApplicantRehab Technology, Inc.
Decision Date1985-04-25
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TELEVISION CONTROL OPTION 1219 is the device name listed in this FDA 510(k) record. The listed applicant is Rehab Technology, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K850313. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEVISION CONTROL OPTION 1219?

TELEVISION CONTROL OPTION 1219 is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Rehab Technology, Inc.. The 510(k) number is K850313.

When did TELEVISION CONTROL OPTION 1219 receive FDA 510(k) clearance?

TELEVISION CONTROL OPTION 1219 received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850313.

Who is the listed applicant for TELEVISION CONTROL OPTION 1219?

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

What is the FDA product code for TELEVISION CONTROL OPTION 1219?

The FDA product code for TELEVISION CONTROL OPTION 1219 is IQA.

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 Rehab Technology, 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.

K921084THE EXCELSIORK850314TELEVISION CONTROL OPTION 1220K840808ECU 1218

Related Devices (Code: IQA)

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.

K961306DELTATALKER WITH INFRAREDPrentke Romich Co.K953905IMPERIUMTeledyne Brown EngineeringK953937LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEMApt Technology, Inc.K943244DEUCEApt Technology, Inc.K944585SCANNING DIRECTORPrentke Romich Co.K944345BEDSIDE BUTLERTrac Medical, 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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