PROVIEW EYE PRESSURE MONITOR— 510(k) K011199
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K011199 for PROVIEW EYE PRESSURE MONITOR, Substantially Equivalent on 2001-07-02. Applicant: Bausch & Lomb, Inc.. Device class: 2.
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code HKY
- Device class
- Class 2
- Regulation
- 21 CFR 886.1930
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rochester, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.