510(k) K932391
K932391 is an FDA 510(k) premarket notification submitted by Navarre Biomedical , Ltd. for the device "NAVARRE BIOMEDICAL UNIVERSAL DRAINAGE CATHETER SET". The FDA issued a decision of Substantially Equivalent on January 27, 1994. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Navarre Biomedical , Ltd. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 27, 1994
- Date Received
- May 18, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type