LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD— 510(k) K884362
Substantially EquivalentBausch & Lomb Pharmaceutical, Inc.
FDA 510(k) clearance K884362 for LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD, Substantially Equivalent on 1988-11-29. Applicant: Bausch & Lomb Pharmaceutical, Inc.. Device class: 2.
Clearance details
- Applicant
- Bausch & Lomb Pharmaceutical, Inc.
- Product code
- Code HQJ
- Device class
- Class 2
- Regulation
- 21 CFR 886.3300
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Clearwater, FL, US
Recent devices under product code HQJ
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