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FDA 510(k)

REMOTE CONTROL SWITCH

K-Number: K900969 · 1990-03-13

ApplicantBaylor Biomedical Services
Decision Date1990-03-13
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REMOTE CONTROL SWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Baylor Biomedical Services. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K900969. 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 REMOTE CONTROL SWITCH?

REMOTE CONTROL SWITCH is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Baylor Biomedical Services. The 510(k) number is K900969.

When did REMOTE CONTROL SWITCH receive FDA 510(k) clearance?

REMOTE CONTROL SWITCH received FDA 510(k) clearance on 1990-03-13, under 510(k) number K900969.

Who is the listed applicant for REMOTE CONTROL SWITCH?

The FDA 510(k) record lists Baylor Biomedical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REMOTE CONTROL SWITCH?

The FDA product code for REMOTE CONTROL SWITCH 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 Baylor Biomedical Services 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.

K901029YES-NO VOICE BOX 7011K901030ROTARY COMMUNICATION SCANNER MODEL 7010K901028ENVIRONMENTAL CONTROL UNIT MODEL 7000

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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