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FDA 510(k)

FLOWMEDIC, MODEL 220

K-Number: K042217 · 2005-01-12

ApplicantFlowmedic (Israel), Ltd.
Decision Date2005-01-12
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLOWMEDIC, MODEL 220 is the device name listed in this FDA 510(k) record. The listed applicant is Flowmedic (Israel), Ltd.. It received FDA 510(k) clearance on 2005-01-12 under 510(k) number K042217. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOWMEDIC, MODEL 220?

FLOWMEDIC, MODEL 220 is a medical device that received FDA 510(k) clearance on 2005-01-12. The listed applicant is Flowmedic (Israel), Ltd.. The 510(k) number is K042217.

When did FLOWMEDIC, MODEL 220 receive FDA 510(k) clearance?

FLOWMEDIC, MODEL 220 received FDA 510(k) clearance on 2005-01-12, under 510(k) number K042217.

Who is the listed applicant for FLOWMEDIC, MODEL 220?

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

What is the FDA product code for FLOWMEDIC, MODEL 220?

The FDA product code for FLOWMEDIC, MODEL 220 is JOW.

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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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