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Calgon Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K944950
KLENZYME
December 20, 1994
K943364
CORASSIST WOUND DRESSING
August 3, 1994
K940263
NPH-KLENZ
May 18, 1994
K935063
INSTRU KLENZ
May 9, 1994
K940407
KALTOGEL WOUND DRESSING
April 7, 1994