510(k) K980193
K980193 is an FDA 510(k) premarket notification submitted by Medical Device Technologies, Inc. for the device "MANAN GENERAL UTILITY DRAINAGE CATHETER". The FDA issued a decision of Substantially Equivalent on May 27, 1998. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Medical Device Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 27, 1998
- Date Received
- January 20, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Nephrostomy
- Device Class
- Class U
- Regulation Number
- Review Panel
- GU
- Submission Type