Infinix INFX-8000V, V6.40— 510(k) K170909
Substantially EquivalentToshiba Medical Systems Coroporation
FDA 510(k) clearance K170909 for Infinix INFX-8000V, V6.40, Substantially Equivalent on 2017-06-16. Applicant: Toshiba Medical Systems Coroporation. Device class: 2.
Clearance details
- Applicant
- Toshiba Medical Systems Coroporation
- Product code
- Code OWB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1650
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Otawara-Shi, JP
Recent devices under product code OWB
view allMore clearances from Toshiba Medical Systems Coroporation
view allAdverse events under product code OWB
product code OWB- Death
- 49
- Injury
- 340
- Malfunction
- 36,973
- Total
- 37,362
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K170909
K-number listed on FDA's recall record- Z-1666-2022 — INFX-8000V. For radiographic and fluoroscopic studies and intervention.
- Z-1174-2021 — System INFX-8000V
- Z-1269-2021 — Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and lower extremities.
- Z-2325-2020 — Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.
- Z-0844-2018 — INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K170909.
Data sourced from openFDA. This site is unofficial and independent of the FDA.