510(k) K050499
K050499 is an FDA 510(k) premarket notification submitted by Life-Tech, Inc. for the device "PROBLOC, HN SERIES AND PROLONG, PL SERIES". The FDA issued a decision of Substantially Equivalent on May 17, 2005. The device falls under product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)), a Class II device regulated under 21 CFR 868.5150. Life-Tech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 17, 2005
- Date Received
- February 28, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Conduction, Anesthetic (W/Wo Introducer)
- Device Class
- Class II
- Regulation Number
- 868.5150
- Review Panel
- AN
- Submission Type