TOSHIBA, SMIT ROENTGEN— 510(k) K873314

Name: FDA 510(k) clearance K873314
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Inland Tube Corp.

FDA 510(k) clearance K873314 for TOSHIBA, SMIT ROENTGEN, Substantially Equivalent on 1987-11-02. Applicant: Inland Tube Corp.. Device class: 1.

Clearance details

Applicant: Inland Tube Corp.
Product code: Code ITY
Device class: Class 1
Regulation: 21 CFR 892.1760
Advisory panel: Radiology
Date received: 1987-08-19
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

Download summary PDF View on FDA.gov ↗

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K923094 — MOLYBDENUM1993-03-04
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K921129 — MRX-7001992-10-05

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.