VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)— 510(k) K993039
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K993039 for VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700), Substantially Equivalent on 2000-01-07. Applicant: Bausch & Lomb, Inc.. Device class: 2.
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code MRH
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.