SA/7860 FETAL HEART MONITOR (DOPPLER)— 510(k) K790951

Name: FDA 510(k) clearance K790951
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

Schlosser Alberti Co.

FDA 510(k) clearance K790951 for SA/7860 FETAL HEART MONITOR (DOPPLER), Substantially Equivalent on 1979-08-03. Applicant: Schlosser Alberti Co.. Device class: 2.

Clearance details

Applicant: Schlosser Alberti Co.
Product code: Code KNG
Device class: Class 2
Regulation: 21 CFR 884.2660
Advisory panel: Obstetrics/Gynecology
Date received: 1979-05-21
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNG

view all

K252669 — Fetal Doppler U8-25, U9-252026-01-08
K242846 — Doppler FHR Detector (BF-500D+, BF-560)2025-06-26
K233823 — Ultrasonic Fetal Doppler2024-06-28
K232893 — Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)2024-06-14
K220245 — Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)2022-09-28

More clearances from Schlosser Alberti Co.

view all

K790950 — S/A 7800 BIRTH SUPPORT CHAIR1979-08-03

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