ALOKA MODEL SSD-650 ULTRASOUND IMAGING SYSTEM— 510(k) K895449

Name: FDA 510(k) clearance K895449
Creator: U.S. Food and Drug Administration
Published: 1990-03-05

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K895449 for ALOKA MODEL SSD-650 ULTRASOUND IMAGING SYSTEM, Substantially Equivalent on 1990-03-05. Applicant: Ge Medical Systems Information Technologies. Device class: 2.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1989-08-23
Decision date: 1990-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HGL

view all

K952031 — ULTRASOUND TRANSDUCER, MODEL US9171995-07-18
K923335 — ULTRASOUND TRANSUCER, MODEL US915 -- MODIFICATION1994-07-22
K924516 — OP3/VP41993-06-28
K903348 — ULTRASONIC PULSED DOPPLER IMAGING SYSTEM1990-10-22
K900966 — EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBE1990-09-12

More clearances from Ge Medical Systems Information Technologies

view all

K120770 — QT GUARD PLUS ANALYSIS SYSTEM2012-12-06
K102426 — CARESCAPE MODEL V100 VITAL SIGNS MONITOR2010-10-20
K092369 — 12SL ECG ANALYSIS PROGRAM2010-02-24
K093141 — MARS HOLTER ANALYSIS WORKSTATION2009-12-29
K092027 — CARESCAPE MONITOR B8502009-08-28

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