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

DRY-FORM

K Number: K872663 · Decision Aug 6, 1987
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
14
Applicant Total
14
Review Days
29

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Basic Information

Device Name
DRY-FORM
K Number
K872663
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Anatech, Ltd.
Date Received
July 8, 1987
Decision Date
August 6, 1987
Product Code
IFP
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
IFP Formalin, Neutral Buffered

Similar 510(k) Clearances

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Other Clearances by Anatech, Ltd.

K Number Device Name
K882873 FIELDTEX HEMATOXYLIN
K882874 ZINC FORMALIN
K882268 ZINC FORMALIN CONCENTRATE
K881282 XYLENE
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. →