SONY DKR-700 DIGITAL STILL RECORDER— 510(k) K961680
Substantially EquivalentSony Medical Systems
FDA 510(k) clearance K961680 for SONY DKR-700 DIGITAL STILL RECORDER, Substantially Equivalent on 1996-07-03. Applicant: Sony Medical Systems. Device class: 1.
Clearance details
- Applicant
- Sony Medical Systems
- 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
- North Attleboro, MA, US
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