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

TECHNICON PARACUT

K Number: K833071 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
10
Applicant Total
157
Review Days
36

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TECHNICON PARACUT
K Number
K833071
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Technicon Instruments Corp.
Date Received
September 8, 1983
Decision Date
October 14, 1983
Product Code
KEO
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
KEO Formulations, Paraffin, All

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KEO), ordered by most recent decision date.

View all

Other Clearances by Technicon Instruments Corp.

K Number Device Name
K914511 TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL
K914888 TECHNICON CHEM 1(TM) SYST (GEN2 SYST)
K914025 TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)
K912616 TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES
K912413 CHEM-LINK DATA BASE MANAGER
K903825 DRUG OF ABUSE ANALYSIS SYSTEM
K903305 TECHNICON CHEM I SYSTEM CARBON DIOXIDE METHOD
K903824 DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY
K903306 TECHNICON CHEM I SYSTEM MAGNESIUM METHOD
K901410 TECHNICON RA-2000(TM) SYSTEM
Search all 157 clearances from Technicon Instruments Corp. →