Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RT-200 COMPUTER INTERFACE

K-Number: K875075 · 1988-04-21

ApplicantTimeter Instrument Corp.
Decision Date1988-04-21
Product CodeBXX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RT-200 COMPUTER INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Timeter Instrument Corp.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K875075. The device is classified under product code BXX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RT-200 COMPUTER INTERFACE?

RT-200 COMPUTER INTERFACE is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K875075.

When did RT-200 COMPUTER INTERFACE receive FDA 510(k) clearance?

RT-200 COMPUTER INTERFACE received FDA 510(k) clearance on 1988-04-21, under 510(k) number K875075.

Who is the listed applicant for RT-200 COMPUTER INTERFACE?

The FDA 510(k) record lists Timeter Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RT-200 COMPUTER INTERFACE?

The FDA product code for RT-200 COMPUTER INTERFACE is BXX.

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 Timeter Instrument Corp. 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.

K875074VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000K871603CRITERION II & IIA OXYGEN CONCENTRATORSK864836L.A.P. SPIROMETERK834274CRITERION IK823775BORDON GAGE REGULATOR #BGK822746RT-200 CALIBRATION ANALYZER

View all 29 devices →

Related Devices (Code: BXX)

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.

K923397SINGLE DOSE GAS INJECTOREscalon Medical TrekK850029UTAH PRESSURE TRANSDUCER CALIBRATOR TRU-CALUtah Medical Products, Inc.K822746RT-200 CALIBRATION ANALYZERTimeter Instrument Corp.K801256NEEDLE COUNTER-SURE COUNT-DISPOSA-TRAYKleen Test ProductsK801258NEEDLE COUNTER-SURE COUNT/10 COUNTKleen Test ProductsK801257NEEDLE COUNTER-SURE COUNT/30 CT. MAGN.Kleen Test Products

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.

↑