FDA 510(k) clearance · back to tracker

LIFEPAK 15 MONITOR/DEFIBRILLATOR

Physio-Control, Inc. cleared K082937 on 2009-03-11, decision: substantially equivalent

K-number

K082937

Sponsor

Physio-Control, Inc.

Device

LIFEPAK 15 MONITOR/DEFIBRILLATOR

Class

Class III

Decision

Substantially Equivalent

Decision date

2009-03-11

Product code

MKJ

Advisory committee

Cardiovascular

Medical specialty

Cardiovascular

Regulation number

870.5310

Official FDA record

Open K082937on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K082937 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.