The following data is part of a premarket notification filed by Numed, Inc. with the FDA for Tyshak Peripheral Balloon Dilation Catheter.
Device ID | K931009 |
510k Number | K931009 |
Device Name: | TYSHAK PERIPHERAL BALLOON DILATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | NUMED, INC. MAIN ST. Hopkinton, NY 12940 |
Contact | Susan D Jones |
Correspondent | Susan D Jones NUMED, INC. MAIN ST. Hopkinton, NY 12940 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-02-19 |
Decision Date | 1993-12-21 |