The following data is part of a premarket notification filed by Horizons Intl. Corp. with the FDA for Horizons Papillotome.
Device ID | K002236 |
510k Number | K002236 |
Device Name: | HORIZONS PAPILLOTOME |
Classification | Unit, Electrosurgical, Endoscopic (with Or Without Accessories) |
Applicant | HORIZONS INTL. CORP. 200 POLITECNICA ST. VILLAS UNIV. PO BOX 250435 Aguadilla, PR 00604 |
Contact | Rafic Saleh |
Correspondent | Rafic Saleh HORIZONS INTL. CORP. 200 POLITECNICA ST. VILLAS UNIV. PO BOX 250435 Aguadilla, PR 00604 |
Product Code | KNS |
CFR Regulation Number | 876.4300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-07-24 |
Decision Date | 2001-01-23 |