SHIMADZU LATERAL C-ARM MH-31— 510(k) K882311

Name: FDA 510(k) clearance K882311
Creator: U.S. Food and Drug Administration
Published: 1988-09-14

Substantially Equivalent

Shimadzu Precision Instruments, Inc.

FDA 510(k) clearance K882311 for SHIMADZU LATERAL C-ARM MH-31, Substantially Equivalent on 1988-09-14. Applicant: Shimadzu Precision Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Shimadzu Precision Instruments, Inc.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1988-06-03
Decision date: 1988-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, 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.