FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INSTANT EOSIN-AQUEOUS

K Number: K893663 · Decision Jun 13, 1989
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
9
Applicant Total
5
Review Days
29

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Basic Information

Device Name
INSTANT EOSIN-AQUEOUS
K Number
K893663
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Shandon, Inc.
Date Received
May 15, 1989
Decision Date
June 13, 1989
Product Code
HYB
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HYB Eosin Y

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Other Clearances by Shandon, Inc.

K Number Device Name
K890984 LINISTAIN SLS
K880240 INSTANT EOSIN-ALCOHOLIC
K873107 INSTANT HEMATOXYLIN
K780261 COVERSLIPPER