VENTRICLEAR II, SPECTRUM VENTRICULAR DRAINAGE CATHETER, MODEL N-VVDC-02-ABRM— 510(k) K071640
Substantially EquivalentCook, Inc.
FDA 510(k) clearance K071640 for VENTRICLEAR II, SPECTRUM VENTRICULAR DRAINAGE CATHETER, MODEL N-VVDC-02-ABRM, Substantially Equivalent on 2007-07-12. Applicant: Cook, Inc.. Device class: 2.
Clearance details
- Applicant
- Cook, Inc.
- Product code
- Code NHC
- Device class
- Class 2
- Regulation
- 21 CFR 882.4100
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Bloomington, IN, US
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Recalls naming K071640
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 K071640.
Data sourced from openFDA. This site is unofficial and independent of the FDA.