MAESTRO DIGITAL VIDEO SYSTEM
FDA 510(k) clearance K920373 · decided 1992-06-24
Clearance details
- K-number
- K920373
- Device name
- MAESTRO DIGITAL VIDEO SYSTEM
- Applicant
- International Imaging Electronics
- Decision
- Substantially Equivalent
- Date received
- 1992-01-29
- Decision date
- 1992-06-24
- Days to decision
- 147 days
- Clearance type
- Traditional
- Product code
- IYO
- Device class
- 2
- Regulation number
- 892.1560
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Addison, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.