GRI-Alleset Veress Needle— 510(k) K172835
Substantially EquivalentGri Medical and Electronic Technology Co., Ltd.
FDA 510(k) clearance K172835 for GRI-Alleset Veress Needle, Substantially Equivalent on 2018-06-11. Applicant: Gri Medical and Electronic Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Gri Medical and Electronic Technology Co., Ltd.
- Product code
- Code HIF
- Device class
- Class 2
- Regulation
- 21 CFR 884.1730
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jiaxing, CN
Recent devices under product code HIF
view allAdverse events under product code HIF
product code HIF- Death
- 19
- Injury
- 578
- Malfunction
- 5,639
- Total
- 6,236
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.