MEGACART— 510(k) K915225

Substantially Equivalent

Siemens Burdick, Inc.

FDA 510(k) clearance K915225 for MEGACART, Substantially Equivalent on 1992-07-01. Applicant: Siemens Burdick, Inc..

Clearance details

Applicant: Siemens Burdick, Inc.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1991-11-20
Decision date: 1992-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miltoon, WI, US

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More clearances from Siemens Burdick, Inc.

K915327 — ELITE II ELECTROCARDIOGRAPH,MODIFIED1992-10-09
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K914969 — E350I ELECTROCARDIOGRAPH1992-03-26
K913518 — TA620 TREADMILL CONTROLLER1991-10-24
K910634 — DC200 DEFIBRILLATOR1991-07-24

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