The following data is part of a premarket notification filed by Numed, Inc. with the FDA for Numed Tyshak Ii And Z-med Ii Ptv Catheters.
| Device ID | K003052 | 
| 510k Number | K003052 | 
| Device Name: | NUMED TYSHAK II AND Z-MED II PTV CATHETERS | 
| Classification | Catheter, Angioplasty, Peripheral, Transluminal | 
| Applicant | NUMED, INC. P.O BOX 129 Nicholville, NY 12965 | 
| Contact | Nichelle R Laflesh | 
| Correspondent | Nichelle R Laflesh NUMED, INC. P.O BOX 129 Nicholville, NY 12965 | 
| Product Code | LIT | 
| CFR Regulation Number | 870.1250 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2000-10-02 | 
| Decision Date | 2000-11-01 |