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IMPLANTABLE PULSE GENERATOR PACEMAKER

FDA premarket approval P940031/S068 · decided 2010-08-13

Approval details

PMA number
P940031
Supplement
S068
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
IMPLANTABLE PULSE GENERATOR PACEMAKER
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Boston Scientific
Date received
2010-07-15
Decision date
2010-08-13
Days to decision
29 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
REVISION OF INSPECTION PROCEDURES FOR CERAMIC CAPACITORS, CERAMIC NETWORKS, AND CERAMIC CAPACITOR ARRAYS.

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510(k) clearances by this applicant

RecordFirmDate
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