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

Synermed ISE Reagents

K Number: K181201 · Decision Jul 10, 2018
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
161
Applicant Total
3
Review Days
64

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
Synermed ISE Reagents
K Number
K181201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1665
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Infrared Laboratory Systems, LLC (Dba Synermed)
Date Received
May 7, 2018
Decision Date
July 10, 2018
Product Code
JGS
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
JGS Electrode, Ion Specific, Sodium

Similar 510(k) Clearances

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

View all

Other Clearances by Infrared Laboratory Systems, LLC (Dba Synermed)

K Number Device Name
K172416 Synermed Opiate Enzyme Immunoassay
K153692 Synermed Glucose Reagent, Synermed IR-1200 Chemistry Analyzer