ALL-PRO 2010— 510(k) K001321

Substantially Equivalent

All-Pro Imaging Corp.

FDA 510(k) clearance K001321 for ALL-PRO 2010, Substantially Equivalent on 2000-05-16. Applicant: All-Pro Imaging Corp.. Device class: 2.

Clearance details

Applicant: All-Pro Imaging Corp.
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 2000-04-26
Decision date: 2000-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hicksville, NY, US

Download summary PDF View on FDA.gov ↗

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More clearances from All-Pro Imaging Corp.

K001314 — MEDSCOPE2000-07-25
K991435 — AII-PRO 100 PLUS AND ALL-PRO 2001999-05-20
K911291 — ALL-PRO 1001991-07-03

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