MONAGHAN RVM, MODEL 761— 510(k) K884942

Name: FDA 510(k) clearance K884942
Creator: U.S. Food and Drug Administration
Published: 1989-06-07

Substantially Equivalent

Monaghan Medical Corp.

FDA 510(k) clearance K884942 for MONAGHAN RVM, MODEL 761, Substantially Equivalent on 1989-06-07. Applicant: Monaghan Medical Corp.. Device class: 2.

Clearance details

Applicant: Monaghan Medical Corp.
Product code: Code BZK
Device class: Class 2
Regulation: 21 CFR 868.1850
Advisory panel: Anesthesiology
Date received: 1988-11-25
Decision date: 1989-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plattsburgh, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BZK

product code BZK

Death: 2
Total: 2

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.