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Neuroinvent, Inc.

FDA Regulatory Profile

Neuroinvent, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 5, 2014.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142470E-Shield Multi-paried Subdermal Needle ElectrodesNovember 5, 2014
K140200E-SHIELD MULTI-PAIRED SUBDERMAL NEEDLE ELECTRODESJuly 18, 2014

FDA data resources