The following data is part of a premarket notification filed by Tick Kit, Inc. with the FDA for Original Tick Kit/1st Aid Kit.
| Device ID | K895767 |
| 510k Number | K895767 |
| Device Name: | ORIGINAL TICK KIT/1ST AID KIT |
| Classification | First Aid Kit With Drug |
| Applicant | TICK KIT, INC. 164 WATERHOLE RD. East Hampton, NY 11937 |
| Contact | Frank Bickley |
| Correspondent | Frank Bickley TICK KIT, INC. 164 WATERHOLE RD. East Hampton, NY 11937 |
| Product Code | LRR |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent - With Drug (SESD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-27 |
| Decision Date | 1989-12-22 |