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FDA 510(k)

FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE

K-Number: K850560 · 1985-04-17

ApplicantPrecision Medical, Inc.
Decision Date1985-04-17
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 1985-04-17 under 510(k) number K850560. 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 FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE?

FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE is a medical device that received FDA 510(k) clearance on 1985-04-17. The listed applicant is Precision Medical, Inc.. The 510(k) number is K850560.

When did FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE receive FDA 510(k) clearance?

FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE received FDA 510(k) clearance on 1985-04-17, under 510(k) number K850560.

Who is the listed applicant for FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE?

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

What is the FDA product code for FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE?

The FDA product code for FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE is CAX.

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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.K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter GroupK862797AIRCO 2000 SERIES FLOWMETERSAirco, 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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