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Microaire

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K915670MICROAIRE MODEL 2600March 18, 1992
K912205MICRO-AIRE ARTHROS SURG BLADES-VARIOUS DYS PROD NOAugust 16, 1991
K912206MICRO-AIRE ARTHROS SURG BLADES-VARIOUS CO PROD NO.August 16, 1991