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..
Clearance details
- Applicant
- Carl Zeiss Meditec, Inc.
- Product code
- Code HLI
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.