GDXPRO— 510(k) K093521
Substantially EquivalentCarl Zeiss Meditec, Inc.
FDA 510(k) clearance K093521 for GDXPRO, Substantially Equivalent on 2009-11-25. Applicant: Carl Zeiss Meditec, Inc..
Clearance details
- Applicant
- Carl Zeiss Meditec, Inc.
- Product code
- Code MYC
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dublin, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.