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

HISTOMATIC SLIDE STAINER, CODE-ON VERSION

K Number: K872916 · Decision Sep 14, 1987
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
20
Applicant Total
89
Review Days
52

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Basic Information

Device Name
HISTOMATIC SLIDE STAINER, CODE-ON VERSION
K Number
K872916
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3800
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Fisher Scientific Co., LLC
Date Received
July 24, 1987
Decision Date
September 14, 1987
Product Code
KPA
Advisory Committee
Pathology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KPA Slide Stainer, Automated

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