Who is the manufacturer of CORDIS ELECTROPHYSIOLOGY STIMULATOR?

Cordis Corp. filed the 510(k) submission for CORDIS ELECTROPHYSIOLOGY STIMULATOR (K844815).

What is the FDA product code for CORDIS ELECTROPHYSIOLOGY STIMULATOR?

JOQ. It is classified under 21 CFR 870.1750 as a Class 2 device in the Cardiovascular panel.

What is the regulatory pathway for CORDIS ELECTROPHYSIOLOGY STIMULATOR?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like CORDIS ELECTROPHYSIOLOGY STIMULATOR?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

CORDIS ELECTROPHYSIOLOGY STIMULATOR

K844815 · Cordis Corp. · JOQ · Jun 11, 1985 · Cardiovascular

Device Facts

Record ID	K844815
Device Name	CORDIS ELECTROPHYSIOLOGY STIMULATOR
Applicant	Cordis Corp.
Product Code	JOQ · Cardiovascular
Decision Date	Jun 11, 1985
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 870.1750
Device Class	Class 2

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