PHASED ARRAY FLEXIBLE CARDIAC COIL— 510(k) K984588

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K984588 for PHASED ARRAY FLEXIBLE CARDIAC COIL, Substantially Equivalent on 1999-02-08. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant
Philips Medical Systems (Cleveland), Inc.
Product code
Code MOS
Device class
Class 2
Regulation
21 CFR 892.1000
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Cleveland, OH, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MOS

view all

More clearances from Philips Medical Systems (Cleveland), Inc.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.