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FDA 510(k)

Snowden-Pencer MicroLap 3mm Laparoscopic Instruments

K-Number: K163615 · 2017-05-04

ApplicantCarefusion 2200, Inc.
Decision Date2017-05-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Snowden-Pencer MicroLap 3mm Laparoscopic Instruments is a medical device manufactured by Carefusion 2200, Inc.. It received FDA 510(k) clearance on 2017-05-04 under approval number K163615. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Snowden-Pencer MicroLap 3mm Laparoscopic Instruments?

Snowden-Pencer MicroLap 3mm Laparoscopic Instruments is a medical device that received FDA 510(k) clearance on 2017-05-04. It is manufactured by Carefusion 2200, Inc.. The 510(k) number is K163615.

When was Snowden-Pencer MicroLap 3mm Laparoscopic Instruments approved by the FDA?

Snowden-Pencer MicroLap 3mm Laparoscopic Instruments received FDA 510(k) clearance on 2017-05-04, under approval number K163615.

What company makes Snowden-Pencer MicroLap 3mm Laparoscopic Instruments?

Snowden-Pencer MicroLap 3mm Laparoscopic Instruments is manufactured by Carefusion 2200, Inc..

What is the FDA product code for Snowden-Pencer MicroLap 3mm Laparoscopic Instruments?

The FDA product code for Snowden-Pencer MicroLap 3mm Laparoscopic Instruments is GEI.

Other Devices by Carefusion 2200, Inc.

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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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