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

ZINC FORMALIN

K Number: K882874 · Decision Jul 28, 1988
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
0
Applicant Total
14
Review Days
17

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Basic Information

Device Name
ZINC FORMALIN
K Number
K882874
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Anatech, Ltd.
Date Received
July 11, 1988
Decision Date
July 28, 1988
Product Code
LDX
Advisory Committee
Pathology
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
LDX Fixative, Metallic Containing

Other Clearances by Anatech, Ltd.

K Number Device Name
K882873 FIELDTEX HEMATOXYLIN
K882268 ZINC FORMALIN CONCENTRATE
K881282 XYLENE
K872663 DRY-FORM
K872498 HARRIS HEMATOXYLIN
K872499 ANATECH HEMATOXYLIN-NORMAL STRENGTH
K872500 ANATECH HEMATOXYLIN-EXTRA STRENGTH
K870852 NBF 10% NEUTRAL BUFFERED FORMALIN
K842862 CB FORMALIN
K842940 CBA FORMALIN
Search all 14 clearances from Anatech, Ltd. →