The following data is part of a premarket notification filed by Biosearch Medical Products, Inc. with the FDA for Enteroclysis Tube.
| Device ID | K923002 |
| 510k Number | K923002 |
| Device Name: | ENTEROCLYSIS TUBE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | BIOSEARCH MEDICAL PRODUCTS, INC. 35 INDUSTRIAL PKWY. P.O. BOX 1700 Somerville, NJ 08876 |
| Contact | Peter Gorky |
| Correspondent | Peter Gorky BIOSEARCH MEDICAL PRODUCTS, INC. 35 INDUSTRIAL PKWY. P.O. BOX 1700 Somerville, NJ 08876 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent - Kit (SESK) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-22 |
| Decision Date | 1994-06-28 |