MEDIVISION SINOSCOPE— 510(k) K971995

Substantially Equivalent

Medivision Scope Service Center, Inc.

FDA 510(k) clearance K971995 for MEDIVISION SINOSCOPE, Substantially Equivalent on 1997-06-26. Applicant: Medivision Scope Service Center, Inc..

Clearance details

Applicant: Medivision Scope Service Center, Inc.
Product code: Code EOB
Advisory panel: Ear, Nose, Throat
Date received: 1997-05-30
Decision date: 1997-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

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Adverse events under product code EOB

product code EOB

Malfunction: 6,143
Total: 6,143

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.