Cleared Special

K151041 - ERBECRYO 2 Cryosurgical Unit with accessories
(FDA 510(k) Clearance)

May 2015
Decision
14d
Days
Class 2
Risk

K151041 is an FDA 510(k) clearance for the ERBECRYO 2 Cryosurgical Unit with accessories. This device is classified as a Unit, Cryosurgical, Accessories (Class II - Special Controls, product code GEH).

Submitted by Erbe USA, Inc. (Marietta, US). The FDA issued a Cleared decision on May 4, 2015, 14 days after receiving the submission on April 20, 2015.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4350.

Submission Details

510(k) Number K151041 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 20, 2015
Decision Date May 04, 2015
Days to Decision 14 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GEH — Unit, Cryosurgical, Accessories
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4350

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