MOVABLE CORE SAFETY GUIDE — Cordis Corp. (510(k) K790258)

Name: MOVABLE CORE SAFETY GUIDE — Cordis Corp. (510(k) K790258)
Creator: DeviceClear

MOVABLE CORE SAFETY GUIDE — Cordis Corp. (510(k) K790258) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: MOVABLE CORE SAFETY GUIDE; Applicant: Cordis Corp.; Clearance track: 510(k).

Device name	MOVABLE CORE SAFETY GUIDE
Applicant	Cordis Corp.
Clearance track	510(k)
Submission number	K790258
Decision	Substantially Equivalent
Decision date	1979-02-23
Date received	1979-02-06
Product code	DQX
Device class	2
Medical specialty	Cardiovascular
Applicant location	IL, US
Source	openFDA device

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$1999/mo

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