NERVUS MONITOR— 510(k) K021185
Substantially EquivalentTaugagreining HF
FDA 510(k) clearance K021185 for NERVUS MONITOR, Substantially Equivalent on 2002-07-12. Applicant: Taugagreining HF. Device class: 2.
Clearance details
- Applicant
- Taugagreining HF
- Product code
- Code OLV
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Recent devices under product code OLV
view allRecalls naming K021185
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 K021185.
Data sourced from openFDA. This site is unofficial and independent of the FDA.