PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE— 510(k) K023700
Substantially EquivalentPrecision Vascular Systems, Inc.
FDA 510(k) clearance K023700 for PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE, Substantially Equivalent on 2002-12-04. Applicant: Precision Vascular Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Precision Vascular Systems, Inc.
- Product code
- Code DQX
- Device class
- Class 2
- Regulation
- 21 CFR 870.1330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- West Valley City, UT, US
Recent devices under product code DQX
view allMore clearances from Precision Vascular Systems, Inc.
view allAdverse events under product code DQX
product code DQX- Death
- 298
- Injury
- 4,385
- Malfunction
- 7,203
- Other
- 5
- Total
- 11,891
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 K023700
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 K023700.
Data sourced from openFDA. This site is unofficial and independent of the FDA.