MONITOR, FETAL, NO. L04-1100— 510(k) K770692

Name: FDA 510(k) clearance K770692
Creator: U.S. Food and Drug Administration
Published: 1977-04-26

Substantially Equivalent

Brattle Instrument Corp.

FDA 510(k) clearance K770692 for MONITOR, FETAL, NO. L04-1100, Substantially Equivalent on 1977-04-26. Applicant: Brattle Instrument Corp.. Device class: 2.

Clearance details

Applicant: Brattle Instrument Corp.
Product code: Code HGM
Device class: Class 2
Regulation: 21 CFR 884.2740
Advisory panel: Obstetrics/Gynecology
Date received: 1977-04-14
Decision date: 1977-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HGM

product code HGM

Death: 35
Malfunction: 478
Total: 513

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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