Atlas FDA

Philips HeartStart FR3 Defibrillator

FDA premarket approval P160028/S002 · decided 2021-01-11

Approval details

PMA number
P160028
Supplement
S002
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Philips HeartStart FR3 Defibrillator
Generic name
Automated external defibrillators (non-wearable)
Applicant
Philips Medical Systems, Inc.
Date received
2020-10-01
Decision date
2021-01-11
Days to decision
102 days
Decision code
APPR
Product code
MKJ
Advisory committee
Cardiovascular
Expedited review
No
Location
Bothell, WA
Statement
Approval of battery cell modifications to the FR3 Rechargeable Battery (model number 989803150241) due to discontinuation of previous battery cells.

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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