7.5 MHZ ENDOVAGINAL PROBE— 510(k) K870709

Name: FDA 510(k) clearance K870709
Creator: U.S. Food and Drug Administration
Published: 1987-03-27

Substantially Equivalent

Philips Ultrasound, Inc.

FDA 510(k) clearance K870709 for 7.5 MHZ ENDOVAGINAL PROBE, Substantially Equivalent on 1987-03-27. Applicant: Philips Ultrasound, Inc.. Device class: 2.

Clearance details

Applicant: Philips Ultrasound, Inc.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1987-02-20
Decision date: 1987-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, 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 Philips Ultrasound, Inc.

view all

K212777 — Collaboration Live2021-09-24
K203406 — Lumify Diagnostic Ultrasound System2021-02-23
K200603 — AAA Model2020-09-20
K201665 — Collaboration Live2020-09-15
K202216 — EPIQ Series Diagnostic Ultrasound Systems2020-09-02

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