ONCOPROBE SYSTEM— 510(k) K884770

Name: FDA 510(k) clearance K884770
Creator: U.S. Food and Drug Administration
Published: 1989-01-04

Substantially Equivalent

Care Wise Medical Products Corp.

FDA 510(k) clearance K884770 for ONCOPROBE SYSTEM, Substantially Equivalent on 1989-01-04. Applicant: Care Wise Medical Products Corp.. Device class: 1.

Clearance details

Applicant: Care Wise Medical Products Corp.
Product code: Code IZD
Device class: Class 1
Regulation: 21 CFR 892.1320
Advisory panel: Radiology
Date received: 1988-11-14
Decision date: 1989-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morgan Hill, CA, US

Download summary PDF View on FDA.gov ↗

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