Capsule Tech Inc.

FDA Regulatory Profile

Capsule Tech Inc. appears in FDA public data with 1 recall, 1 510(k) clearance, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2377-2012, Class II) was initiated on August 10, 2012. Its most recent 510(k) clearance was granted on June 27, 2012.

Summary

Total Recalls
1
510(k) Clearances
1
Inspections
4
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2377-2012Class IICapsule Neuron Docking Station, a component in the DataCaptor Connectivity System Catalog Number DCAugust 10, 2012

Recent 510(k) Clearances

K-NumberDeviceDate
K113835DATACAPTOR SYSTEMJune 27, 2012