Capintec Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943072BETA C COUNTERSeptember 29, 1994
K935539CAPINTEC CRC 35RFebruary 18, 1994
K930962CAPTUS 2000 WEL COUNTERMay 18, 1993
K924586CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWAREDecember 3, 1992
K921428CAPTUS 500May 28, 1992
K910020CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELSApril 8, 1991
K905796DOSE CALIBRATORMarch 18, 1991