MALE/MALE LUER TRANSFER TUBING— 510(k) K932780

Name: FDA 510(k) clearance K932780
Creator: U.S. Food and Drug Administration
Published: 1994-01-24

Substantially Equivalent

Innovations For Mechanical Ventilation, Inc.

FDA 510(k) clearance K932780 for MALE/MALE LUER TRANSFER TUBING, Substantially Equivalent on 1994-01-24. Applicant: Innovations For Mechanical Ventilation, Inc.. Device class: 1.

Clearance details

Applicant: Innovations For Mechanical Ventilation, Inc.
Product code: Code CAI
Device class: Class 1
Regulation: 21 CFR 868.5240
Advisory panel: Anesthesiology
Date received: 1993-06-09
Decision date: 1994-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New City, NY, US

Download summary PDF View on FDA.gov ↗

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K932781 — DUAL VALVED RESPIRATORY T1994-01-24
K923800 — PRESSURE GAUGE1993-02-26

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.