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

VITAHEAT PATIENT WARMING SYSTEM

K Number: K132454 · Decision Oct 4, 2013
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
1
Review Days
59

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
VITAHEAT PATIENT WARMING SYSTEM
K Number
K132454
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vitaheat Medical, LLC
Date Received
August 6, 2013
Decision Date
October 4, 2013
Product Code
DWJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
DWJ System, Thermal Regulating

Similar 510(k) Clearances

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

View all