OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM— 510(k) K901118
Substantially EquivalentAdac Laboratories
FDA 510(k) clearance K901118 for OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM, Substantially Equivalent on 1990-04-10. Applicant: Adac Laboratories. Device class: 1.
Clearance details
- Applicant
- Adac Laboratories
- Product code
- Code LMB
- Device class
- Class 1
- Regulation
- 21 CFR 892.2010
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milpitas, CA, US
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