X-RAY TUBE, ROTATING ANODE— 510(k) K770336

Name: FDA 510(k) clearance K770336
Creator: U.S. Food and Drug Administration
Published: 1977-03-01

Substantially Equivalent

Litton Medical Systems

FDA 510(k) clearance K770336 for X-RAY TUBE, ROTATING ANODE, Substantially Equivalent on 1977-03-01. Applicant: Litton Medical Systems. Device class: 1.

Clearance details

Applicant: Litton Medical Systems
Product code: Code ITY
Device class: Class 1
Regulation: 21 CFR 892.1760
Advisory panel: Radiology
Date received: 1977-02-18
Decision date: 1977-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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
K923094 — MOLYBDENUM1993-03-04
K923141 — PHILIPS PRE-FILTER OPTION1993-01-21
K921129 — MRX-7001992-10-05

More clearances from Litton Medical Systems

view all

K770333 — FLUOROSCOPE, C-ARM1977-03-01
K770334 — TILTING X-RAY TABLE1977-03-01
K770337 — FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.1977-03-01
K770338 — X-RAY CONTROL & X-RAY HV GENERATOR1977-03-01
K770335 — COLLIMATOR, AUTOMATIC1977-02-28

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.