KNIGHTSTAR 335— 510(k) K973004

Substantially Equivalent

Puritan Bennett Corp.

FDA 510(k) clearance K973004 for KNIGHTSTAR 335, Substantially Equivalent on 1998-07-16. Applicant: Puritan Bennett Corp..

Clearance details

Applicant: Puritan Bennett Corp.
Product code: Code MNT
Advisory panel: Anesthesiology
Date received: 1997-08-13
Decision date: 1998-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

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Adverse events under product code MNT

product code MNT

Death: 118
Injury: 324
Malfunction: 25,451
Other: 2
Total: 25,895

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.