3MHZ ANNULAR ARRAY— 510(k) K864980

Substantially Equivalent

Philips Ultrasound, Inc.

FDA 510(k) clearance K864980 for 3MHZ ANNULAR ARRAY, Substantially Equivalent on 1987-05-11. Applicant: Philips Ultrasound, Inc.. Device class: 2.

Clearance details

Applicant: Philips Ultrasound, Inc.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1986-12-22
Decision date: 1987-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

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