SONICAID MODEL TEAM FECG IUP— 510(k) K930714

Name: FDA 510(k) clearance K930714
Creator: U.S. Food and Drug Administration
Published: 1995-08-24

Substantially Equivalent

Oxford Instruments, Plc.

FDA 510(k) clearance K930714 for SONICAID MODEL TEAM FECG IUP, Substantially Equivalent on 1995-08-24. Applicant: Oxford Instruments, Plc.. Device class: 2.

Clearance details

Applicant: Oxford Instruments, Plc.
Product code: Code HEL
Device class: Class 2
Regulation: 21 CFR 884.2660
Advisory panel: Obstetrics/Gynecology
Date received: 1993-02-11
Decision date: 1995-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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