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

Infinity Delta, Infinity Delta XL, Infinity Kappa

K Number: K152407 · Decision Sep 23, 2015
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
424
Applicant Total
2
Review Days
29

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
Infinity Delta, Infinity Delta XL, Infinity Kappa
K Number
K152407
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Draeger Medical Sytems, Inc.
Date Received
August 25, 2015
Decision Date
September 23, 2015
Product Code
MHX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Similar 510(k) Clearances

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

View all

Other Clearances by Draeger Medical Sytems, Inc.

K Number Device Name
K172154 Isolette 8000 plus