FDA 510(k)

LAPARETTE, MODEL LAP J L S H N

K-Number: K022979 · 2002-12-18

ApplicantInstruments Medicaux G.B., Inc.

Decision Date2002-12-18

Product CodeKNF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LAPARETTE, MODEL LAP J L S H N is the device name listed in this FDA 510(k) record. The listed applicant is Instruments Medicaux G.B., Inc.. It received FDA 510(k) clearance on 2002-12-18 under 510(k) number K022979. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPARETTE, MODEL LAP J L S H N?

LAPARETTE, MODEL LAP J L S H N is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Instruments Medicaux G.B., Inc.. The 510(k) number is K022979.

When did LAPARETTE, MODEL LAP J L S H N receive FDA 510(k) clearance?

LAPARETTE, MODEL LAP J L S H N received FDA 510(k) clearance on 2002-12-18, under 510(k) number K022979.

Who is the listed applicant for LAPARETTE, MODEL LAP J L S H N?

The FDA 510(k) record lists Instruments Medicaux G.B., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPARETTE, MODEL LAP J L S H N?

The FDA product code for LAPARETTE, MODEL LAP J L S H N is KNF.

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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.