Who is the manufacturer of CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,?

Cordis Corp. filed the PMA application for CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A, (P800040).

What is the FDA product code for CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,?

LGW. as a Class 3 device in the Neurology panel.

Who can help prepare an FDA PMA submission like CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA PMA submissions. See https://innolitics.com/services/regulatory/ or contact https://innolitics.com/contact.

CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,

P800040 · Cordis Corp. · LGW · Apr 14, 1981 · Neurology

Device Facts

Record ID	P800040
Device Name	CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,
Applicant	Cordis Corp.
Product Code	LGW · Neurology
Decision Date	Apr 14, 1981
Decision	APWD
Device Class	Class 3

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