FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

LapBox Power Tissue Containment System

K Number: K250212 · Decision Apr 15, 2025
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
3
Applicant Total
1
Review Days
81

Basic Information

Device Name
LapBox Power Tissue Containment System
K Number
K250212
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4050
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARK Surgical
Date Received
January 24, 2025
Decision Date
April 15, 2025
Product Code
PMU
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PMU Containment System, Laparoscopic Power Morcellation, With Instrument Port

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