The following data is part of a premarket notification filed by Lake Medical Products, Inc. with the FDA for Lake Catheter Care Kit.
| Device ID | K872750 |
| 510k Number | K872750 |
| Device Name: | LAKE CATHETER CARE KIT |
| Classification | Catheter, Urological |
| Applicant | LAKE MEDICAL PRODUCTS, INC. 11866 ADIE RD. Maryland Heights, MO 63043 |
| Contact | Eli Schachet |
| Correspondent | Eli Schachet LAKE MEDICAL PRODUCTS, INC. 11866 ADIE RD. Maryland Heights, MO 63043 |
| Product Code | KOD |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-13 |
| Decision Date | 1987-09-03 |