VERI-VU LENSOMETER— 510(k) K791521
Substantially EquivalentIntermedics, Inc.
FDA 510(k) clearance K791521 for VERI-VU LENSOMETER, Substantially Equivalent on 1979-10-30. Applicant: Intermedics, Inc.. Device class: 1.
Clearance details
- Applicant
- Intermedics, Inc.
- Product code
- Code HLM
- Device class
- Class 1
- Regulation
- 21 CFR 886.1425
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.