DITER ULTRASONIC S 3000— 510(k) K901950

Substantially Equivalent

Diter Elektroniikka OY

FDA 510(k) clearance K901950 for DITER ULTRASONIC S 3000, Substantially Equivalent on 1990-07-27. Applicant: Diter Elektroniikka OY. Device class: 2.

Clearance details

Applicant: Diter Elektroniikka OY
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1990-05-01
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IMI

K240788 — Ultrasound Stimulator2025-06-04
K230472 — Sonopuls 1902023-10-24
K222098 — ManaSport+2023-03-08
K210284 — ManaSport2022-04-26
K202788 — Sonomed IV, Sonomed V2021-12-23

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