The following data is part of a premarket notification filed by Cook Urological, Inc. with the FDA for Silicone Foley Catheter.
Device ID | K951106 |
510k Number | K951106 |
Device Name: | SILICONE FOLEY CATHETER |
Classification | Catheter, Retention Type, Balloon |
Applicant | COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
Contact | Darcy Job |
Correspondent | Darcy Job COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
Product Code | EZL |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-10 |
Decision Date | 1995-05-25 |