KELMAN(TM) OMNIFIT II MODEL 2100
FDA premarket approval P850059 · decided 1986-07-31
Approval details
- PMA number
- P850059
- Trade name
- KELMAN(TM) OMNIFIT II MODEL 2100
- Generic name
- intraocular lens
- Applicant
- Bausch & Lomb Surgical, Inc.
- Date received
- 1985-08-15
- Decision date
- 1986-07-31
- Days to decision
- 350 days
- Decision code
- APWD
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Rochester, NY
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