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FDA 510(k)

FLOWMETER NIPPLE ADAPTOR

K-Number: K934945 · 1993-11-17

ApplicantCardio-Search , Ltd.
Decision Date1993-11-17
Product CodeCCN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOWMETER NIPPLE ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cardio-Search , Ltd.. It received FDA 510(k) clearance on 1993-11-17 under 510(k) number K934945. The device is classified under product code CCN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOWMETER NIPPLE ADAPTOR?

FLOWMETER NIPPLE ADAPTOR is a medical device that received FDA 510(k) clearance on 1993-11-17. The listed applicant is Cardio-Search , Ltd.. The 510(k) number is K934945.

When did FLOWMETER NIPPLE ADAPTOR receive FDA 510(k) clearance?

FLOWMETER NIPPLE ADAPTOR received FDA 510(k) clearance on 1993-11-17, under 510(k) number K934945.

Who is the listed applicant for FLOWMETER NIPPLE ADAPTOR?

The FDA 510(k) record lists Cardio-Search , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOWMETER NIPPLE ADAPTOR?

The FDA product code for FLOWMETER NIPPLE ADAPTOR is CCN.

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Related Devices (Code: CCN)

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.

K920783OXYGEN FLOW CONTROLLERPuritan Bennett Corp.K872038NEB-U-VENTDesign Technologies, Inc.K871262MODIFIED NOFLO IDesign Technologies, Inc.K863613NO-FLO IDesign Technologies, Inc.K863659FLOW INTERRUPTION INDICATORSalter LabsK863657OXYGEN CONSERVATORSalter Labs

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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