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Spica, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K800801ANALGESIA UNITS, OXYGEN & NITRATE DEVICEMay 28, 1980
K780364MANIFOLD KITMarch 30, 1978
K780365OXYGEN/NITROUS OXIDE OUTLETMarch 30, 1978