MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000— 510(k) K882323

Substantially Equivalent

Meicor, Inc.

FDA 510(k) clearance K882323 for MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000, Substantially Equivalent on 1988-06-30. Applicant: Meicor, Inc..

Clearance details

Applicant: Meicor, Inc.
Product code: Code ITY
Advisory panel: Radiology
Date received: 1988-06-06
Decision date: 1988-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

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Adverse events under product code ITY

product code ITY

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.