The following data is part of a premarket notification filed by Suredrop, Inc. with the FDA for Suredrop Eyedrop Guide.
| Device ID | K874569 |
| 510k Number | K874569 |
| Device Name: | SUREDROP EYEDROP GUIDE |
| Classification | Gauge, Measuring |
| Applicant | SUREDROP, INC. P.O. BOX 123 Tiger, GA 30576 |
| Contact | William Smith |
| Correspondent | William Smith SUREDROP, INC. P.O. BOX 123 Tiger, GA 30576 |
| Product Code | JYJ |
| CFR Regulation Number | 874.4420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-05 |
| Decision Date | 1988-05-03 |