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

AUTODILUTER III

K Number: K810659 · Decision Mar 31, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
27
Review Days
20

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Basic Information

Device Name
AUTODILUTER III
K Number
K810659
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2500
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Dynatech Corp.
Date Received
March 11, 1981
Decision Date
March 31, 1981
Product Code
JTC
Advisory Committee
Microbiology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
JTC Device, Microtiter Diluting/Dispensing

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Other Clearances by Dynatech Corp.

K Number Device Name
K904567 DYNATECH MR4000 MICROPLATE READER
K854603 MULTI MASH 2000
K854604 AUTO MASH
K854602 MINI MASH 2000
K832117 IMMULON SUBSTRATE REMOVAWELL STRIPS
K823787 HANDI-WASH
K823833 MICRO STIX #011-010-5000 & HOLDER#5100
K830200 MICROELISA MINIREADER II
K823773 PROVIAL II #006-010-0201
K823557 REMOVAWELL PLATE LID
Search all 27 clearances from Dynatech Corp. →