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FDA 510(k)

CLASSIC (TM) 200 OXYGEN FLOWMETER

K-Number: K871452 · 1987-06-22

ApplicantThe Timeter Group
Decision Date1987-06-22
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLASSIC (TM) 200 OXYGEN FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is The Timeter Group. It received FDA 510(k) clearance on 1987-06-22 under 510(k) number K871452. The device is classified under product code CAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLASSIC (TM) 200 OXYGEN FLOWMETER?

CLASSIC (TM) 200 OXYGEN FLOWMETER is a medical device that received FDA 510(k) clearance on 1987-06-22. The listed applicant is The Timeter Group. The 510(k) number is K871452.

When did CLASSIC (TM) 200 OXYGEN FLOWMETER receive FDA 510(k) clearance?

CLASSIC (TM) 200 OXYGEN FLOWMETER received FDA 510(k) clearance on 1987-06-22, under 510(k) number K871452.

Who is the listed applicant for CLASSIC (TM) 200 OXYGEN FLOWMETER?

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

What is the FDA product code for CLASSIC (TM) 200 OXYGEN FLOWMETER?

The FDA product code for CLASSIC (TM) 200 OXYGEN FLOWMETER is CAX.

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 The Timeter Group 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.

K862171MP-500 ELECTRONIC NEBULIZERK852374OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18K844556KHM 2000 DRIP WATCHER

Related Devices (Code: CAX)

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.

K923781MXR-2000 FLOWMETERPorter Instrument Co., Inc.K910316OHMEDA - LOW FLOW FLOWMETEROhmeda MedicalK884973FR6000 FLOWMETERKey InstrumentsK872718SERIES D FLOWMETERPuritan Bennett Corp.K862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.K854067SELECT FLOWMETERPrecision 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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