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FDA 510(k)

FUNNEL GUIDE CATHETER MODEL G1020608

K-Number: K102439 · 2012-01-12

ApplicantLazarus Effect, Inc.
Decision Date2012-01-12
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FUNNEL GUIDE CATHETER MODEL G1020608 is the device name listed in this FDA 510(k) record. The listed applicant is Lazarus Effect, Inc.. It received FDA 510(k) clearance on 2012-01-12 under 510(k) number K102439. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUNNEL GUIDE CATHETER MODEL G1020608?

FUNNEL GUIDE CATHETER MODEL G1020608 is a medical device that received FDA 510(k) clearance on 2012-01-12. The listed applicant is Lazarus Effect, Inc.. The 510(k) number is K102439.

When did FUNNEL GUIDE CATHETER MODEL G1020608 receive FDA 510(k) clearance?

FUNNEL GUIDE CATHETER MODEL G1020608 received FDA 510(k) clearance on 2012-01-12, under 510(k) number K102439.

Who is the listed applicant for FUNNEL GUIDE CATHETER MODEL G1020608?

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

What is the FDA product code for FUNNEL GUIDE CATHETER MODEL G1020608?

The FDA product code for FUNNEL GUIDE CATHETER MODEL G1020608 is DQY.

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Related Devices (Code: DQY)

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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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