VISX EXCIMER LASER SYSTEM MODELS B AND C
FDA premarket approval P930016/S001 · decided 1996-10-15
Approval details
- PMA number
- P930016
- Supplement
- S001
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- VISX EXCIMER LASER SYSTEM MODELS B AND C
- Generic name
- Excimer laser system
- Applicant
- Amo Manufacturing USA, LLC
- Date received
- 1996-04-18
- Decision date
- 1996-10-15
- Days to decision
- 180 days
- Decision code
- APPR
- Product code
- LZS
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Milpitas, CA
- Statement
- LABELING CHANGES (I.E., MINOR EDITORAL CHANGES TO THE PATIENT INFORMATION BOOKLET, CONTRAST SENSITIVITY/GLARE PRECAUTIONARY STATEMENT IN LIEU OF A POSTAPPROVAL CONTRAST SENSITIVITY STUDY, AND DEFINITIONS OF POTENTIAL RISKS WITH PRK)
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.
510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| Catalys™ Precision Laser System (K223838) | Amo Manufacturing USA, LLC | 2023-04-12 |
| CATALYS Precision Laser system (K220516) | Amo Manufacturing USA, LLC | 2022-05-17 |
| CATALYS Precision Laser System (K210701) | Amo Manufacturing USA, LLC | 2021-04-07 |
| Catalys Precision Laser System (K182083) | Amo Manufacturing USA, LLC | 2018-11-09 |
| Catalys Precision Laser System (K172002) | Amo Manufacturing USA, LLC | 2017-08-25 |
| IFS ADVANCED FEMTOSECOND LASER SYSTEM (K141852) | Amo Manufacturing USA, LLC | 2015-01-06 |