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

MICROREADER 4

K Number: K935983 · Decision Dec 9, 1994
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
8
Review Days
360

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
MICROREADER 4
K Number
K935983
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hyperion, Inc.
Date Received
December 14, 1993
Decision Date
December 9, 1994
Product Code
JJQ
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

Similar 510(k) Clearances

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

View all

Other Clearances by Hyperion, Inc.

K Number Device Name
K022800 VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM
K013213 HYPERION VISIQUANT ANA TEST KIT
K913809 HY-PREP SYSTEM
K873138 MICRO-READER II
K864060 MICRO-READER
K855149 COMPUTING SPECTROPHOTOMETER BIO-CHEMISTRY ANALYZER
K834071 LYMPHANGIOGRAPHY SET SPECIAL 30G