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

THE PURPLE IRIS(TM) CYTOPATHOLOGY WORKSTATION

K Number: K874207 · Decision Jan 5, 1988
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
8
Applicant Total
14
Review Days
82

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Basic Information

Device Name
THE PURPLE IRIS(TM) CYTOPATHOLOGY WORKSTATION
K Number
K874207
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3600
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Intl. Remote Imaging Systems
Date Received
October 15, 1987
Decision Date
January 5, 1988
Product Code
IBJ
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
IBJ Light, Microscope

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Other Clearances by Intl. Remote Imaging Systems

K Number Device Name
K022774 IQ 200 SYSTEM
K000373 939UDX URINE PATHOLOGY SYSTEM
K972141 THE YELLOW IRIS URINALYSIS WORKSTATION
K953116 WHITE IRIS LEUKOCYTE DIFFERENTIAL ANALYZER
K960054 900UDX URINE PATHOLOGY SYSTEM
K954006 YELLOW IRIS URINALYSIS WORKSTATION W/IRISCOPE BODY FLUID ANALYSIS CAPABILITY
K943463 THE YELLOW IRIS
K934539 THE YELLOW IRIS URINALYSIS WORKSTATION WITH IRISCOPE BODY FLUID ANALYSIS CAPABILITY
K914256 YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU
K893530 IRISTAIN FORMULA 2, PARTS 1 AND 2
Search all 14 clearances from Intl. Remote Imaging Systems →