REGULATOR, PRESSURE, CUFF— 510(k) K760453

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K760453 for REGULATOR, PRESSURE, CUFF, Substantially Equivalent on 1976-09-13. Applicant: Boehringer Laboratories.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code JOH
Advisory panel: Anesthesiology
Date received: 1976-08-16
Decision date: 1976-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code JOH

product code JOH

Death: 42
Injury: 1,344
Malfunction: 5,608
Other: 1
Total: 6,995

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.