510(k) K182086
K182086 is an FDA 510(k) premarket notification submitted by A.T.S. Applicazione Tecnologie Speciali S.R.L. for the device "ARCO FP". The FDA issued a decision of Substantially Equivalent on August 20, 2019. The device falls under product code OWB (Interventional Fluoroscopic X-Ray System), a Class II device regulated under 21 CFR 892.1650. A.T.S. Applicazione Tecnologie Speciali S.R.L. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 20, 2019
- Date Received
- August 2, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Interventional Fluoroscopic X-Ray System
- Device Class
- Class II
- Regulation Number
- 892.1650
- Review Panel
- RA
- Submission Type
Interventional fluoroscopy