HEARTSTART MRX MONITOR/DEFIBRILLATOR— 510(k) K062233

Substantially Equivalent

Philips Medical Systems North America, Inc.

FDA 510(k) clearance K062233 for HEARTSTART MRX MONITOR/DEFIBRILLATOR, Substantially Equivalent on 2006-11-22. Applicant: Philips Medical Systems North America, Inc.. Device class: 3.

Clearance details

Applicant
Philips Medical Systems North America, Inc.
Product code
Code MKJ
Device class
Class 3
Regulation
21 CFR 870.5310
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Andover, MA, US
Download summary PDFView on FDA.gov ↗

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More clearances from Philips Medical Systems North America, Inc.

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Adverse events under product code MKJ

product code MKJ
Death
961
Injury
1,070
Malfunction
90,719
Other
8
Total
92,758

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K062233

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K062233.

Data sourced from openFDA. This site is unofficial and independent of the FDA.