PMA P160022S030

Decision date
1969-12-31

Current openFDA PMA Record

Device
X Series, AED Pro, Propaq MD
Applicant
ZOLL Medical Corporation
PMA number
P160022
Supplement
S030
Product code
MKJ
Generic name
Automated external defibrillators (non-wearable)
Decision date
2021-08-13
Decision code
OK30
Date received
2021-08-06
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Addition of an alternate soldering machine, replacement of an existing wash machine, replacement of an existing ionograph machine, and replacement of existing IC manual programming.

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