5.0 MHZ Convex Array Intravaginal Transducer

FDA 510(k) K895123 · Advanced Technology Laboratories, Inc.

Substantially Equivalent

510(k) numberK895123

Submission

Device name
5.0 MHZ Convex Array Intravaginal Transducer
Applicant
Advanced Technology Laboratories, Inc.
Bothell, WA, US
Received
August 15, 1989
Decision date
November 13, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HGL – Transducer, Ultrasonic, Obstetric
Device class
Class II (moderate risk)
Regulation
21 CFR 884.2960
Specialty
Obstetrics/Gynecology

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K900966EUP-V12 5.0 MHZ Convex Array Transvaginal ProbeHGL · Traditional Hitachi Medical Corp. of America09/12/1990SE
K903316Aloka UST-964P-5 Endovaginal TransducerHGL · Traditional Ge Medical Systems Information Technologies08/22/1990SE
K901142Mer Multiplane Vaginal Probe (MVP)HGL · Traditional Medical Equipment Resources08/22/1990SE
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K895449Aloka Model SSD-650 Ultrasound Imaging SystemHGL · Traditional Ge Medical Systems Information Technologies03/05/1990SE
K881263Model 500A Vascular Spectrum Analyzer W/DopplerHGL · Traditional Multigon Industries, Inc.01/05/1990SE

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Questions and answers

When was 5.0 MHZ Convex Array Intravaginal Transducer cleared by the FDA?

5.0 MHZ Convex Array Intravaginal Transducer (K895123) received a 510(k) decision of Substantially Equivalent on November 13, 1989, 90 days after the submission was received.

What is the product code of K895123?

The FDA product code is HGL – Transducer, Ultrasonic, Obstetric, a Class II (moderate risk) device regulated under 21 CFR 884.2960.