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Reichert-Jung, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K864821
AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2
February 10, 1987
K862551
FUNS-10, FUNS-11
September 12, 1986
K852994
REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11
July 29, 1985