ClearanceBrief
Company ยท US

Shandon, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1989. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HYBEosin Y2
HYKHematoxylin Harris'S1
KIMDevice For Sealing Microsections1
KIOSlide Stainer, Immersion Type1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 13, 1989K893663INSTANT EOSIN-AQUEOUS
Shandon, Inc.
HYB
Apr 4, 1989K890984LINISTAIN SLS
Shandon, Inc.
KIO
Mar 3, 1988K880240INSTANT EOSIN-ALCOHOLIC
Shandon, Inc.
HYB
Aug 21, 1987K873107INSTANT HEMATOXYLIN
Shandon, Inc.
HYK
Apr 18, 1978K780261COVERSLIPPER
Shandon, Inc.
KIM

Latest recalls

DateFirm and productCodeLinked 510(k)
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