510(k) K121720

Device
WELKINS EMT/ICU TEMPERATURE MANAGERMENT SYSTEM
Applicant
WELKINS, LLC
510(k) number
K121720
Product code
DWJ  
Decision
Substantially Equivalent (SESE)
Decision date
2012-08-20
Date received
2012-06-12
Regulation
870.5900
Classification name
System, Thermal Regulating
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
CHRISTOPHER BLODGETT
Address
1430 Blue Oaks Blvd. Suite 250 Roseville CA US 95747 95747

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
B9301610000WelkinsWELKINS, LLC2021-03-03

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Legacy Summary

summary

FDA Review

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