MOLYBDENUM— 510(k) K923094

Name: FDA 510(k) clearance K923094
Creator: U.S. Food and Drug Administration
Published: 1993-03-04

Substantially Equivalent

Southeastern Medical Diagnostics, Inc.

FDA 510(k) clearance K923094 for MOLYBDENUM, Substantially Equivalent on 1993-03-04. Applicant: Southeastern Medical Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Southeastern Medical Diagnostics, Inc.
Product code: Code ITY
Device class: Class 1
Regulation: 21 CFR 892.1760
Advisory panel: Radiology
Date received: 1992-06-25
Decision date: 1993-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greensboro, NC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ITY

view all

K000052 — X-RAY MONOBLOCK, MONOBLOCK XRS-60-3302000-02-10
K933162 — MRX-7501993-10-07
K923141 — PHILIPS PRE-FILTER OPTION1993-01-21
K921129 — MRX-7001992-10-05
K921130 — MRX-8651992-09-10

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.