510(k) K170741
K170741 is an FDA 510(k) premarket notification submitted by Geotek Medikal Ltd Sti for the device "GTK Disposable Needle Guides". The FDA issued a decision of Substantially Equivalent on Jun 1, 2017. The device falls under product code ITX (Transducer, Ultrasonic, Diagnostic), a Class II device regulated under 21 CFR 892.1570. Geotek Medikal Ltd Sti has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 1, 2017
- Date Received
- Mar 10, 2017
- 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
- 510(k)