AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE— 510(k) K873359

Name: FDA 510(k) clearance K873359
Creator: U.S. Food and Drug Administration
Published: 1987-11-06

Substantially Equivalent

American Pharmaseal Div. Ahsc

FDA 510(k) clearance K873359 for AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE, Substantially Equivalent on 1987-11-06. Applicant: American Pharmaseal Div. Ahsc. Device class: 1.

Clearance details

Applicant: American Pharmaseal Div. Ahsc
Product code: Code CAI
Device class: Class 1
Regulation: 21 CFR 868.5240
Advisory panel: Anesthesiology
Date received: 1987-08-21
Decision date: 1987-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAI

product code CAI

Malfunction: 869
Other: 1
Total: 870

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.