MODIFIED SINGLE PATIENT USE DISP MAN RESUSCITATOR— 510(k) K903443

Substantially Equivalent

Puritan Bennett Corp.

FDA 510(k) clearance K903443 for MODIFIED SINGLE PATIENT USE DISP MAN RESUSCITATOR, Substantially Equivalent on 1990-08-17. Applicant: Puritan Bennett Corp..

Clearance details

Applicant: Puritan Bennett Corp.
Product code: Code BTM
Advisory panel: Anesthesiology
Date received: 1990-07-31
Decision date: 1990-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

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Adverse events under product code BTM

product code BTM

Death: 19
Other: 2
Total: 21

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.