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

10% NEUTRAL BUFFERED FORMALIN CONCENT

K Number: K812940 · Decision Dec 10, 1981
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
14
Applicant Total
12
Review Days
51

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Basic Information

Device Name
10% NEUTRAL BUFFERED FORMALIN CONCENT
K Number
K812940
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Surgipath
Date Received
October 20, 1981
Decision Date
December 10, 1981
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

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Other Clearances by Surgipath

K Number Device Name
K820027 MODIFIED EA 50
K812087 EA 50
K812086 EA 65
K811825 ORANGE G-6
K811826 EOSIN Y
K810836 DECALCIFIER II
K810758 GILL'S HEMATOXYLIN #1
K810733 HARRIS HEMATOXYLIN
K810759 GILL'S HEMATOXYLIN #2
K810760 GILL'S HEMATOXYLIN #3
Search all 12 clearances from Surgipath →