Transvaginal Transducer, 5MHZ

FDA 510(k) K860234 · Philips Medical Systems, Inc.

Substantially Equivalent

510(k) numberK860234

Submission

Device name
Transvaginal Transducer, 5MHZ
Applicant
Philips Medical Systems, Inc.
Santa Ana, CA, US
Received
January 22, 1986
Decision date
May 23, 1986
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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K924516OP3/VP4HGL · Traditional Huntleigh Technology, Inc.06/28/1993SE
K903348Ultrasonic Pulsed Doppler Imaging SystemHGL · Traditional Advanced Technology Laboratories, Inc.10/22/1990SE
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
K900838Transvaginal Transducer AssemblyHGL · Traditional Pie Medical Equipment B.V.05/23/1990SE
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 Transvaginal Transducer, 5MHZ cleared by the FDA?

Transvaginal Transducer, 5MHZ (K860234) received a 510(k) decision of Substantially Equivalent on May 23, 1986, 121 days after the submission was received.

What is the product code of K860234?

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