OCULINUM INJECTION AMPLIFIER— 510(k) K900279
Substantially EquivalentOculinum, Inc.
FDA 510(k) clearance K900279 for OCULINUM INJECTION AMPLIFIER, Substantially Equivalent on 1990-02-09. Applicant: Oculinum, Inc.. Device class: 2.
Clearance details
- Applicant
- Oculinum, Inc.
- Product code
- Code HLW
- Device class
- Class 2
- Regulation
- 21 CFR 886.1640
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Berkeley, CA, US
Recent devices under product code HLW
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