ENDOSTAR(TM) STYLET— 510(k) K933598

Substantially Equivalent

Fiberoptic Medical Products, Inc.

FDA 510(k) clearance K933598 for ENDOSTAR(TM) STYLET, Substantially Equivalent on 1994-01-25. Applicant: Fiberoptic Medical Products, Inc..

Clearance details

Applicant: Fiberoptic Medical Products, Inc.
Product code: Code BSR
Advisory panel: Anesthesiology
Date received: 1993-07-26
Decision date: 1994-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allentown, PA, US

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Adverse events under product code BSR

product code BSR

Death: 2
Other: 1
Total: 3

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.