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Artel, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K933836
HBM HEMOGLOBINOMETER
March 31, 1994
K920914
MP/S SINGLE WAVELENGTH MINI PHOTOMETER
March 23, 1992
K914809
MP MINI PHOTOMETER
January 27, 1992
K864542
ARTEL DIFFERENTIAL PHOTOMETER
February 6, 1987