FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TECHNICON H*1 SYSTEMS, LABFACTS SOFTWARE FOR U.I.W. VERSIONS 4.11 & 5.11

K Number: K933478 · Decision Nov 22, 1993
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
11
Review Days
129

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 H*1 SYSTEMS, LABFACTS SOFTWARE FOR U.I.W. VERSIONS 4.11 & 5.11
K Number
K933478
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Miles, Inc.
Date Received
July 16, 1993
Decision Date
November 22, 1993
Product Code
GKZ
Advisory Committee
Hematology
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
GKZ Counter, Differential Cell

Similar 510(k) Clearances

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

View all

Other Clearances by Miles, Inc.

K Number Device Name
K950292 FOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM, IN VITRO DIAGNOSTIC SYSTEM
K950353 TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
K950186 CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
K945655 CREATININE (ENZYMATIC UV) PROCEDURE FOR TECHNICON SYSTEMS (IN VITRO DIAGNOSTIC TEST SYSTEM)
K941171 TECHNICON H* 3 RTC SYSTEM (IN-VITRO DIAGNOSTIC SYSTEM)
K943376 OPERA SYSTEM
K941156 TECHNISON AXON SYSTEM
K933682 DIRECT AMYLASE (EC 3.2.1.1) METHOD FOR TECHNICON SYSTEMS
K935287 IRON -II (FE-II) METHOD/TECH CHEM 1(R) 1+TM SYSTEM
K933475 TECHNICON H* 2 SYSTEM, LABFACTS SOFTWARE FOR U.I.W. VERSIONS 4.11 & 5.11
Search all 11 clearances from Miles, Inc. →