Cleared Traditional

K142207 - TransferMan 4m Micromanipulator (FDA 510(k) Clearance)

Jan 2015
Decision
165d
Days
Class 2
Risk

K142207 is an FDA 510(k) clearance for the TransferMan 4m Micromanipulator. This device is classified as a Micromanipulators And Microinjectors, Assisted Reproduction (Class II - Special Controls, product code MQJ).

Submitted by Eppendorf AG (Hamburg, DE). The FDA issued a Cleared decision on January 23, 2015, 165 days after receiving the submission on August 11, 2014.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.6150.

Submission Details

510(k) Number K142207 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 11, 2014
Decision Date January 23, 2015
Days to Decision 165 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code MQJ — Micromanipulators And Microinjectors, Assisted Reproduction
Device Class Class II - Special Controls
CFR Regulation 21 CFR 884.6150

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