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

ISOSCAN

K Number: K944185 · Decision Nov 17, 1994
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
17
Applicant Total
44
Review Days
83

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
ISOSCAN
K Number
K944185
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2400
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Isolab, Inc.
Date Received
August 26, 1994
Decision Date
November 17, 1994
Product Code
JQT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JQT Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica

Similar 510(k) Clearances

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

View all

Other Clearances by Isolab, Inc.

K Number Device Name
K951014 ISOLAB'S T4 TEST KIT
K950481 NEONATAL CHEMISTRY SYSTEM, GALACTOSE TEST KIT
K943547 PHENYLALANINE TEST KIT
K950803 ISOLAB'S GALACTOSE-1-PHOSPHATE URIDYL TRANFERASE TEST KITS 800, 4000 SAMPLE
K950415 FLUOROSCAN NEONATAL
K942276 QUIK-SEP QUANTITATIVE HEMOGLOBIN S ASSAY
K942222 QUIK-SEP QUANTITIVE HEMOGLOBIN S CONTROLS
K934013 RESOLVE SYSTEMS ALKALINE PHOSPHATASE TEST KIT
K923153 HEMOCARD, HEMOGLOBIN C ASSAY
K931234 HEMOCARD CONTROL HB-AA, AE, FAA, FAE
Search all 44 clearances from Isolab, Inc. →