The following data is part of a premarket notification filed by Lake Medical Products, Inc. with the FDA for Lake N/g Feeding Tube.
| Device ID | K884127 |
| 510k Number | K884127 |
| Device Name: | LAKE N/G FEEDING TUBE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| 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 | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-30 |
| Decision Date | 1989-02-08 |