LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)— 510(k) K761210

Name: FDA 510(k) clearance K761210
Creator: U.S. Food and Drug Administration
Published: 1976-12-21

Substantially Equivalent

Physio-Control Corp.

FDA 510(k) clearance K761210 for LIMB LEAD SEL. (ECG LEAD SWITCHING AD.), Substantially Equivalent on 1976-12-21. Applicant: Physio-Control Corp.. Device class: 2.

Clearance details

Applicant: Physio-Control Corp.
Product code: Code DRW
Device class: Class 2
Regulation: 21 CFR 870.2350
Advisory panel: Cardiovascular
Date received: 1976-12-07
Decision date: 1976-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DRW

view all

K033513 — EASI ECG ALGORITHM2004-01-15
K020456 — EASI 12 LEAD ALGORITHM2002-07-09
K930786 — EPCOR1994-09-26
K872781 — EASI LEAD SYSTEM CABLE ASSEMBLY1987-12-29
K861981 — ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTOR1986-08-25

More clearances from Physio-Control Corp.

view all

K991910 — LIFEPAK 12 BIPHASIC1999-09-03
K990338 — NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM1999-09-01
K983393 — LIFEPAK 500 BIPHASIC1999-05-05
K973486 — LIFE PAK 121998-01-09
K962359 — LIFEPAK 3001997-11-06

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