Cappel Diagnostics, Inc.

FDA Regulatory Profile

Cappel Diagnostics, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 20, 1987.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K872839ANTINUCLEAR ANTIBODY TESTOctober 20, 1987
K864275ANTI-NDNA ANTIBODY TEST KITDecember 15, 1986
K862821CAPPEL DIAGNOSTICS ANA KITAugust 15, 1986