510(k) K122983
K122983 is an FDA 510(k) premarket notification submitted by KARL STORZ Endoscopy-America, Inc. for the device "KSEA BIPOLAR ELECTRODE". The FDA issued a decision of Substantially Equivalent on June 26, 2013. The device falls under product code HIN (Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)), a Class II device regulated under 21 CFR 884.4150. KARL STORZ Endoscopy-America, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 26, 2013
- Date Received
- September 26, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)
- Device Class
- Class II
- Regulation Number
- 884.4150
- Review Panel
- OB
- Submission Type