The following data is part of a premarket notification filed by Medical Device Technologies, Inc. with the FDA for Manan General Utility Drainage Catheter.
| Device ID | K980193 |
| 510k Number | K980193 |
| Device Name: | MANAN GENERAL UTILITY DRAINAGE CATHETER |
| Classification | Catheter, Nephrostomy |
| Applicant | MEDICAL DEVICE TECHNOLOGIES, INC. 4445 SW 35TH TERRACE SUITE 310 Gainesville, FL 32608 |
| Contact | Karl Swartz |
| Correspondent | Karl Swartz MEDICAL DEVICE TECHNOLOGIES, INC. 4445 SW 35TH TERRACE SUITE 310 Gainesville, FL 32608 |
| 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 | 1998-01-20 |
| Decision Date | 1998-05-27 |
| Summary: | summary |