P2020 MOBILE C-ARM IMAGE INTENSIFIER— 510(k) K874905

Name: FDA 510(k) clearance K874905
Creator: U.S. Food and Drug Administration
Published: 1988-02-26

Substantially Equivalent

Photo Medic Equipment, Inc.

FDA 510(k) clearance K874905 for P2020 MOBILE C-ARM IMAGE INTENSIFIER, Substantially Equivalent on 1988-02-26. Applicant: Photo Medic Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Photo Medic Equipment, Inc.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1987-12-01
Decision date: 1988-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bay Shore, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JAA

product code JAA

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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