IOLMaster 700— 510(k) K173771
Substantially EquivalentCarl Zeiss Meditec, AG
FDA 510(k) clearance K173771 for IOLMaster 700, Substantially Equivalent on 2018-08-24. Applicant: Carl Zeiss Meditec, AG. Device class: 2.
Clearance details
- Applicant
- Carl Zeiss Meditec, AG
- Product code
- Code HJO
- Device class
- Class 2
- Regulation
- 21 CFR 886.1850
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jena, DE
Recent devices under product code HJO
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view allRecalls naming K173771
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K173771.
Data sourced from openFDA. This site is unofficial and independent of the FDA.