MOBETRON— 510(k) K981112
Substantially EquivalentIntraop Medical, Inc.
FDA 510(k) clearance K981112 for MOBETRON, Substantially Equivalent on 1998-07-24. Applicant: Intraop Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Intraop Medical, Inc.
- Product code
- Code LHN
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
Recent devices under product code LHN
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