Machida America, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K871712MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.January 14, 1988
K854581MACHIDA SEMI-RIGID BRONCHOSCOPE FBS-6R-50February 28, 1986
K844834MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1June 11, 1985
K841087FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000May 16, 1984
K821182MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-May 13, 1982
K821181FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #May 13, 1982
K812734MACHIDA FLEXIBLE INTUBATION SCOPE FLS-POctober 19, 1981
K811943MACHIDA NASOPHARYNGO-LARYNGOSCOPEJuly 28, 1981