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510(k) K880442

Device
BRUSHRITE
Applicant
PRO CARE LABORATORIES, INC.
510(k) number
K880442
Product code
JEG  
Decision
Substantially Equivalent (SESE)
Decision date
1988-05-16
Date received
1988-02-02
Regulation
868.1075
Classification name
Analyzer, Gas, Argon, Gaseous-phase
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
EUGENE M MUELLER
Address
218 W. Park St. West Point NE US 68788 68788

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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