BR 2002 X-RAY GENERATOR SYSTEM— 510(k) K801808

Name: FDA 510(k) clearance K801808
Creator: U.S. Food and Drug Administration
Published: 1980-09-26

Substantially Equivalent

Valmet Indus. Mach. & Prod., Inc.

FDA 510(k) clearance K801808 for BR 2002 X-RAY GENERATOR SYSTEM, Substantially Equivalent on 1980-09-26. Applicant: Valmet Indus. Mach. & Prod., Inc.. Device class: 1.

Clearance details

Applicant: Valmet Indus. Mach. & Prod., Inc.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1980-07-30
Decision date: 1980-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K952265 — MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR1995-07-06

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