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FDA 510(k)

MODEL CF-300 THREE CHANNEL FLOW METER

K-Number: K792190 · 1979-11-21

ApplicantWilton Webster Laboratories
Decision Date1979-11-21
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL CF-300 THREE CHANNEL FLOW METER is the device name listed in this FDA 510(k) record. The listed applicant is Wilton Webster Laboratories. It received FDA 510(k) clearance on 1979-11-21 under 510(k) number K792190. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL CF-300 THREE CHANNEL FLOW METER?

MODEL CF-300 THREE CHANNEL FLOW METER is a medical device that received FDA 510(k) clearance on 1979-11-21. The listed applicant is Wilton Webster Laboratories. The 510(k) number is K792190.

When did MODEL CF-300 THREE CHANNEL FLOW METER receive FDA 510(k) clearance?

MODEL CF-300 THREE CHANNEL FLOW METER received FDA 510(k) clearance on 1979-11-21, under 510(k) number K792190.

Who is the listed applicant for MODEL CF-300 THREE CHANNEL FLOW METER?

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

What is the FDA product code for MODEL CF-300 THREE CHANNEL FLOW METER?

The FDA product code for MODEL CF-300 THREE CHANNEL FLOW METER is DRQ.

Related Clinical Trials

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Other records listing Wilton Webster Laboratories 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.

K780131THERMOMETER, DIGITAL, NTM-100

Related Devices (Code: DRQ)

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.

K172216ACIST RXi Mini SystemAcist Medical Systems, Inc.K050006BOREALIS AMPLIFIER (CLEARSIGN), MODEL 2001232 160 CHANNEL VERSION, 2001267 80 CHANNEL VERSION, 2001268 40 CHANNEL VERSIOC.R. Bard, Inc.K050974DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERSDraeger Medical Systems, Inc.K033807INFINITYEDICAL INFORMATION BUS (MIB/MIB II AND MIB DUO) PROTOCOL CONVERTERDraeger Medical Systems, Inc.K013205MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000Millar Instruments, Inc.K020277SIEMENS MEDICAL INFROMATION BUS (MIB II) PROTOCOL CONVERTERSiemens Medical Solutions USA, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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