PALLADIUM SEED MODEL 100— 510(k) K852542

Name: FDA 510(k) clearance K852542
Creator: U.S. Food and Drug Administration
Published: 1986-01-14

Substantially Equivalent

Nuclear Medicine, Inc.

FDA 510(k) clearance K852542 for PALLADIUM SEED MODEL 100, Substantially Equivalent on 1986-01-14. Applicant: Nuclear Medicine, Inc.. Device class: 2.

Clearance details

Applicant: Nuclear Medicine, Inc.
Product code: Code IWI
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 1985-06-14
Decision date: 1986-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IWI

view all

K973363 — NORTH AMERICAN SCIENTIFIC(NASI)PD-103 RADIONUCLIDE BRACHYTHERAPY SOURCE-MODEL MED36331998-07-02
K940632 — I-125 RAPID STRAND1994-09-02
K912170 — RADIOACTIVE IODINE-125 SOURCES1991-08-09
K882449 — CESIUM 137 SOURCE, MODEL CSM-401989-04-14
K874787 — MODIFIED PALLADIUM SEED MODEL 1001987-12-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.