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Shandon, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K893663
INSTANT EOSIN-AQUEOUS
June 13, 1989
K890984
LINISTAIN SLS
April 4, 1989
K880240
INSTANT EOSIN-ALCOHOLIC
March 3, 1988
K873107
INSTANT HEMATOXYLIN
August 21, 1987
K780261
COVERSLIPPER
April 18, 1978