ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON— 510(k) K926454

Name: FDA 510(k) clearance K926454
Creator: U.S. Food and Drug Administration
Published: 1993-06-22

Unknown

Medical, Inc.

FDA 510(k) clearance K926454 for ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON, Unknown on 1993-06-22. Applicant: Medical, Inc.. Device class: 1.

Clearance details

Applicant: Medical, Inc.
Product code: Code CAI
Device class: Class 1
Regulation: 21 CFR 868.5240
Advisory panel: Anesthesiology
Date received: 1992-12-24
Decision date: 1993-06-22
Decision: Unknown
Clearance type: Traditional
Location: San Francisco, 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.