ANESTHESIOLOGY DEVICES— 510(k) K820046

Substantially Equivalent

Bentley Laboratories, Inc.

FDA 510(k) clearance K820046 for ANESTHESIOLOGY DEVICES, Substantially Equivalent on 1982-01-29. Applicant: Bentley Laboratories, Inc..

Clearance details

Applicant: Bentley Laboratories, Inc.
Product code: Code DRS
Advisory panel: Cardiovascular
Date received: 1982-01-07
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DRS

product code DRS

Death: 8
Malfunction: 776
Total: 784

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.