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 | Device Class | Medical Specialty |
|---|---|---|---|
| PMU | Containment System, Laparoscopic Power Morcellation, With Instrument Port | FDA class 2 | Obstetrics/Gynecology |
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