SURGICAL IOP MONITOR— 510(k) K863235
Substantially EquivalentAmeritek, Inc.
FDA 510(k) clearance K863235 for SURGICAL IOP MONITOR, Substantially Equivalent on 1986-09-25. Applicant: Ameritek, Inc.. Device class: 2.
Clearance details
- Applicant
- Ameritek, Inc.
- Product code
- Code HKX
- Device class
- Class 2
- Regulation
- 21 CFR 886.1930
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seattle, WA, US
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