UPSHERSCOPE(TM)— 510(k) K922275

Substantially Equivalent

Upsher Laryngoscope Co.

FDA 510(k) clearance K922275 for UPSHERSCOPE(TM), Substantially Equivalent on 1993-01-06. Applicant: Upsher Laryngoscope Co..

Clearance details

Applicant: Upsher Laryngoscope Co.
Product code: Code CCW
Advisory panel: Anesthesiology
Date received: 1992-05-14
Decision date: 1993-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

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Adverse events under product code CCW

product code CCW

Death: 31
Injury: 136
Malfunction: 3,703
Other: 1
Total: 3,871

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.