OCTAX LASER SHOT SYSTEM— 510(k) K062524
Substantially EquivalentMinitube of America, Inc.
FDA 510(k) clearance K062524 for OCTAX LASER SHOT SYSTEM, Substantially Equivalent on 2006-12-15. Applicant: Minitube of America, Inc.. Device class: 2.
Clearance details
- Applicant
- Minitube of America, Inc.
- Product code
- Code MRX
- Device class
- Class 2
- Regulation
- 21 CFR 884.6200
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Verona, WI, US
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More clearances from Minitube of America, Inc.
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