510(k) K163502
K163502 is an FDA 510(k) premarket notification submitted by Biobot Surgical Pte., Ltd. for the device "iSR'obot Biopsy Kit". The FDA issued a decision of Substantially Equivalent on May 16, 2017. The device falls under product code ITX (Transducer, Ultrasonic, Diagnostic), a Class II device regulated under 21 CFR 892.1570. Biobot Surgical Pte., Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 16, 2017
- Date Received
- December 14, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transducer, Ultrasonic, Diagnostic
- Device Class
- Class II
- Regulation Number
- 892.1570
- Review Panel
- RA
- Submission Type