ADULT ANESTHESIA BREATHING CIRCUIT KITS— 510(k) K934462

Unknown

Zefon Medical Products

FDA 510(k) clearance K934462 for ADULT ANESTHESIA BREATHING CIRCUIT KITS, Unknown on 1994-03-01. Applicant: Zefon Medical Products.

Clearance details

Applicant: Zefon Medical Products
Product code: Code CAI
Advisory panel: Anesthesiology
Date received: 1993-09-13
Decision date: 1994-03-01
Decision: Unknown
Clearance type: Traditional
Location: Ocala, FL, US

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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.