Lifepak 5 Cardioscope Module (NPN 5)

FDA 510(k) K760677 · Physio-Control Corp.

Substantially Equivalent

510(k) numberK760677

Submission

Device name
Lifepak 5 Cardioscope Module (NPN 5)
Applicant
Physio-Control Corp.
Mchenry, IL, US
Received
September 20, 1976
Decision date
October 5, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DPS – Electrocardiograph
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2340
Specialty
Cardiovascular

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K142430LIFEPAK 15 monitor/defibrillatorMKJ · Traditional 12/19/2014SE
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K122600Lifepak 1000 DefibrillatorMKJ · Traditional 10/11/2012SE
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Questions and answers

When was Lifepak 5 Cardioscope Module (NPN 5) cleared by the FDA?

Lifepak 5 Cardioscope Module (NPN 5) (K760677) received a 510(k) decision of Substantially Equivalent on October 5, 1976, 15 days after the submission was received.

What is the product code of K760677?

The FDA product code is DPS – Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2340.