3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT— 510(k) K912225
Substantially Equivalent3M Medical Products Group
FDA 510(k) clearance K912225 for 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT, Substantially Equivalent on 1991-07-22. Applicant: 3M Medical Products Group. Device class: 2.
Clearance details
- Applicant
- 3M Medical Products Group
- Product code
- Code IXW
- Device class
- Class 2
- Regulation
- 21 CFR 892.1900
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St Paul, MN, US
Recent devices under product code IXW
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