Atlas FDA

HV splitter/adaptor kit 5019

FDA premarket approval P920015/S202 · decided 2017-09-05

Approval details

PMA number
P920015
Supplement
S202
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
HV splitter/adaptor kit 5019
Generic name
Permanent defibrillator electrodes
Applicant
Medtronic, Inc.
Date received
2017-08-09
Decision date
2017-09-05
Days to decision
27 days
Decision code
OK30
Product code
NVY
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Change from manual to robotic automation of the application of adhesive to adaptor housing halves.

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