Atlas FDA

HeartStart FR3 Defibrillator

FDA premarket approval P160028/S001 · decided 2020-08-03

Approval details

PMA number
P160028
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
HeartStart FR3 Defibrillator
Generic name
Automated external defibrillators (non-wearable)
Applicant
Philips Medical Systems, Inc.
Date received
2020-07-06
Decision date
2020-08-03
Days to decision
28 days
Decision code
OK30
Product code
MKJ
Advisory committee
Cardiovascular
Expedited review
No
Location
Bothell, WA
Statement
Changes to the inspection procedure for components and sub-assemblies used to build the HeartStart family of defibrillators.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
PCR ELEVA 1.2 (K093355)Philips Medical Systems, Inc.2010-01-08
PINNACLE3 SMARTARC (K090808)Philips Medical Systems, Inc.2009-04-03
PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 (K071391)Philips Medical Systems, Inc.2007-09-07
PHILIPS REUSABLE SPO2 SENSORS M1191T, M1192T AND M1193T, CLIP SENSOR M1196T AND DISPOSABLE SPO2 SENSORS M1131A, M1132A (K063783)Philips Medical Systems, Inc.2007-04-27
M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE F.0 AND M4840A PHILIPS TELEMETRY SYSTEM II INCLUDING M4841A PATIEN (K041741)Philips Medical Systems, Inc.2004-07-21
M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE E.01 AND INTELLIVUE CLINICAL NETWORK ON VLAN (K040955)Philips Medical Systems, Inc.2004-05-12
HEARTSTART MRX, MODEL M3535A (K040404)Philips Medical Systems, Inc.2004-05-04
M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE F.O AND THE M4840A TELEMETRY MONITORING SYSTEM II (K040357)Philips Medical Systems, Inc.2004-03-03