PEGASUS BIWAVE SYSTEM— 510(k) K933004

Substantially Equivalent

Pegasus Airwave, Inc.

FDA 510(k) clearance K933004 for PEGASUS BIWAVE SYSTEM, Substantially Equivalent on 1994-03-07. Applicant: Pegasus Airwave, Inc..

Clearance details

Applicant: Pegasus Airwave, Inc.
Product code: Code FNM
Advisory panel: General Hospital
Date received: 1993-06-21
Decision date: 1994-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerfield Beach, FL, US

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Adverse events under product code FNM

product code FNM

Death: 22
Injury: 349
Other: 4
Total: 375

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.