MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122— 510(k) K040228
Substantially EquivalentMedi-Stim A/S
FDA 510(k) clearance K040228 for MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122, Substantially Equivalent on 2004-04-29. Applicant: Medi-Stim A/S. Device class: 2.
Clearance details
- Applicant
- Medi-Stim A/S
- Product code
- Product code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Brooklyn Park, MN, US
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More clearances from Medi-Stim A/S
view allRecalls naming K040228
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 K040228.
Data sourced from openFDA. This site is unofficial and independent of the FDA.