SUTUREGROOVE— 510(k) K994289
Substantially EquivalentIop, Inc.
FDA 510(k) clearance K994289 for SUTUREGROOVE, Substantially Equivalent on 2000-04-17. Applicant: Iop, Inc.. Device class: 2.
Clearance details
- Applicant
- Iop, Inc.
- Product code
- Code MML
- Device class
- Class 2
- Regulation
- 21 CFR 886.5700
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Costa Mesa, CA, US
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More clearances from Iop, Inc.
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