The following data is part of a premarket notification filed by Manan Medical Products, Inc. with the FDA for Manan General Utility Drainage Catheter.
| Device ID | K953713 |
| 510k Number | K953713 |
| Device Name: | MANAN GENERAL UTILITY DRAINAGE CATHETER |
| Classification | Catheter, Nephrostomy |
| Applicant | MANAN MEDICAL PRODUCTS, INC. 2200 CARLSON DR. Northbrook, IL 60062 |
| Contact | Michael Plishka |
| Correspondent | Michael Plishka MANAN MEDICAL PRODUCTS, INC. 2200 CARLSON DR. Northbrook, IL 60062 |
| Product Code | LJE |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-19 |
| Decision Date | 1996-03-26 |