EASI 12 LEAD ALGORITHM— 510(k) K020456

Substantially Equivalent

Philips Medical Systems

FDA 510(k) clearance K020456 for EASI 12 LEAD ALGORITHM, Substantially Equivalent on 2002-07-09. Applicant: Philips Medical Systems. Device class: 2.

Clearance details

Applicant
Philips Medical Systems
Product code
Code DRW
Device class
Class 2
Regulation
21 CFR 870.2350
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Oxnard, CA, US
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