WILCOR-XR RP-OG MEDICAL FILM— 510(k) K834612

Substantially Equivalent

Cea America Corp.

FDA 510(k) clearance K834612 for WILCOR-XR RP-OG MEDICAL FILM, Substantially Equivalent on 1984-02-27. Applicant: Cea America Corp.. Device class: 1.

Clearance details

Applicant: Cea America Corp.
Product code: Code IWZ
Device class: Class 1
Regulation: 21 CFR 892.1840
Advisory panel: Radiology
Date received: 1983-12-20
Decision date: 1984-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IWZ

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K931604 — 3M MEDICAL DIAGNOSTIC VIDEOCASSETTE1993-07-21
K931605 — 3M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE1993-07-20
K920539 — ORWO X-RAY FILM1992-06-30

More clearances from Cea America Corp.

K942525 — MEDICOUNT DEKA HEMATOLOGY ANALYZER1996-06-05
K834613 — WILCOR-XR RP MEDICAL FILM1984-03-05
K834614 — WILCOR-XR RP-L MEDICAL FILM1984-03-05
K834611 — SINGUL-XR RP NON SCREEN MED. FILM1984-02-21

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