IISIS, VERSION 1.0— 510(k) K052244
Substantially EquivalentInnovision Medical Technologies, LLC
FDA 510(k) clearance K052244 for IISIS, VERSION 1.0, Substantially Equivalent on 2005-10-13. Applicant: Innovision Medical Technologies, LLC. Device class: 2.
Clearance details
- Applicant
- Innovision Medical Technologies, LLC
- Product code
- Code MOD
- Device class
- Class 2
- Regulation
- 21 CFR 868.5895
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Linthicum, MD, US
Recent devices under product code MOD
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