Accutorr 7/VS-900 Vital Signs Monitor— 510(k) K170712
Substantially EquivalentShenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
FDA 510(k) clearance K170712 for Accutorr 7/VS-900 Vital Signs Monitor, Substantially Equivalent on 2017-08-02. Applicant: Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
- Product code
- Code MWI
- Device class
- Class 2
- Regulation
- 21 CFR 870.2300
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code MWI
view allMore clearances from Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
view all- K221267 — VS 8 Vital Signs Monitor, VS 8A Vital Signs Monitor, VS 9 Vital Signs Monitor
- K222754 — ViewMate Multi Ultrasound System
- K202785 — Resona R9,Resona R9 Exp,Resona R9 Pro,Resona R9S, Nuewa R9,Nuewa R9 Exp,Nuewa R9 Pro,Nuewa R9S,Resona 7,Resona 7CV,Resona 7EXP,Resona 7S, Resona 7OB,Resona 7PRO,Imagyn 7,Resona Y Diagnostic Ultrasound System
- K173369 — DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System
- K171233 — Resona 7/Resona 7CV/Resona 7EXP/Resona 7S/Resona 7OB Diagnostic Ultrasound System
Adverse events under product code MWI
product code MWI- Death
- 16
- Malfunction
- 963
- Total
- 979
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 K170712
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K170712.
Data sourced from openFDA. This site is unofficial and independent of the FDA.