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

3M SPOTON TEMPERATURE MONITORING SYSTEM

K Number: K120412 · Decision May 30, 2012
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
6
Review Days
110

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
3M SPOTON TEMPERATURE MONITORING SYSTEM
K Number
K120412
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arizant Healthcare, Inc.
Date Received
February 10, 2012
Decision Date
May 30, 2012
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FLL Continuous Measurement Thermometer

Similar 510(k) Clearances

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

View all

Other Clearances by Arizant Healthcare, Inc.

K Number Device Name
K082217 RANGER RAPID FLOW BLOOD/FLUID WARMING SYSTEM
K060939 RANGER IRRIGATION FLUID WARMING SYSTEM
K060865 BAIR PAWS TEMPERATURE MANAGEMENT SYSTEM MODEL 850
K053645 MODIFICATION TO:BAIR HUGGER TEMPERATURE MANAGEMENT SYSTEMS
K041686 BAIR HUGGER TEMPERATURE MANAGEMENT SYSTEM