SONY LASER VIDEODISC RECORDING SYSTEM— 510(k) K921275
Substantially EquivalentSony Medical Systems
FDA 510(k) clearance K921275 for SONY LASER VIDEODISC RECORDING SYSTEM, Substantially Equivalent on 1992-06-10. Applicant: Sony Medical Systems.
Clearance details
- Applicant
- Sony Medical Systems
- Product code
- Code LMB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Attleboro, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.