ANGIOSCAN (AS STAND ALONE INSTRUMENT)— 510(k) K951132
Substantially EquivalentCarl Zeiss Meditec, Inc.
FDA 510(k) clearance K951132 for ANGIOSCAN (AS STAND ALONE INSTRUMENT), Substantially Equivalent on 1995-06-26. Applicant: Carl Zeiss Meditec, Inc.. Device class: 2.
Clearance details
- Applicant
- Carl Zeiss Meditec, Inc.
- Product code
- Code HLI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1570
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code HLI
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