510(k) K833646
K833646 is an FDA 510(k) premarket notification submitted by Edward Weck, Inc. for the device "PULSATRON NERVE LOCATOR/STIMULATOR". The FDA issued a decision of Substantially Equivalent on February 10, 1984. The device falls under product code ETN (Stimulator, Nerve), a Class II device regulated under 21 CFR 874.1820. Edward Weck, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 1984
- Date Received
- October 17, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Nerve
- Device Class
- Class II
- Regulation Number
- 874.1820
- Review Panel
- EN
- Submission Type