Remel, L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972359REMEL BILE ESCULIN AZIDE AGAR W/6 MCG/ML VANCOMYCINAugust 28, 1997
K964315REMEL STAPH LATEX KITFebruary 7, 1997
K964421REMEL MEROPENEM 10UG SUSCEPTIBILITY DISKDecember 6, 1996
K96104610B ARGININE BROTHSeptember 18, 1996
K955143RPR LIQUID CONTROLSJuly 30, 1996
K955136RPR CARD TEST KITJuly 29, 1996
K961819STREPTOMYCIN DISK (300MCG)July 10, 1996
K961818GENTAMICIN DISK (120MCG)July 10, 1996
K960313MUELLER HINTON AGAR WITH 2% NACIMarch 25, 1996
K954986GC BASE W/ 1% GCHIFebruary 16, 1996