The following data is part of a premarket notification filed by Ryder Intl. Corp. with the FDA for Ryder Lacrimal Intubationset.
| Device ID | K962151 |
| 510k Number | K962151 |
| Device Name: | RYDER LACRIMAL INTUBATIONSET |
| Classification | Lacrimal Stents And Intubation Sets |
| Applicant | RYDER INTL. CORP. 1426 CURT FRANCIS RD. Arab, AL 35016 |
| Contact | Dan Clark |
| Correspondent | Dan Clark RYDER INTL. CORP. 1426 CURT FRANCIS RD. Arab, AL 35016 |
| Product Code | OKS |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-04 |
| Decision Date | 1996-09-18 |
| Summary: | summary |