INTER-SHARP— 510(k) K862070
Substantially EquivalentIntermedics Intraocular, Inc.
FDA 510(k) clearance K862070 for INTER-SHARP, Substantially Equivalent on 1986-06-17. Applicant: Intermedics Intraocular, Inc.. Device class: 1.
Clearance details
- Applicant
- Intermedics Intraocular, Inc.
- Product code
- Code HNW
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Passadena, CA, US
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