IMEXDOP CT+— 510(k) K942441

Substantially Equivalent

Imex Medical Systems, Inc.

FDA 510(k) clearance K942441 for IMEXDOP CT+, Substantially Equivalent on 1994-08-23. Applicant: Imex Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Imex Medical Systems, Inc.
Product code: Product code JAF
Device class: Class 2
Regulation: 21 CFR 892.1540
Advisory panel: Radiology
Date received: 1994-05-23
Decision date: 1994-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Golden, CO, US

Download summary PDF View on FDA.gov ↗

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More clearances from Imex Medical Systems, Inc.

K973556 — IMEX MEDICAL SYSTEMS, INC. IMEXLAB 90001998-04-24
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K973336 — IMEX STETHODOP1998-02-05
K970156 — IMEX FUTURALDOP PRO1997-04-04
K942243 — IMEX 8000 PERSONAL CASCULAR LAB1995-11-03

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