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

TISSUE PROCESSING SYSTEM

K Number: K801513 · Decision Jul 28, 1980
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
11
Applicant Total
22
Review Days
28

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Basic Information

Device Name
TISSUE PROCESSING SYSTEM
K Number
K801513
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3875
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Innovative Medical Systems, Inc.
Date Received
June 30, 1980
Decision Date
July 28, 1980
Product Code
IEO
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
IEO Processor, Tissue, Automated

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Other Clearances by Innovative Medical Systems, Inc.

K Number Device Name
K973035 VIOLA II DENTAL CAMERA SYSTEM
K951469 BAZOOKA SYSTEM
K933184 POSITIVE AIRWAY PRESSURE SYSTEM
K924590 MICROWAVE AUTOMATED TISSUE PROCESSOR
K922081 LABOTECH AUTOMATED MICROTITER ANALYZER
K921005 AUTOLOADER
K915457 PHACO 20/20 SYSTEM I
K915456 PHACO 3000 LINEAR
K883599 LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)
K880745 LX-100 SLIDE STAINER
Search all 22 clearances from Innovative Medical Systems, Inc. →