PRECISION OPTICS IMAGE BEAMSPLITTER (COUPLER)— 510(k) K903457

Name: FDA 510(k) clearance K903457
Creator: U.S. Food and Drug Administration
Published: 1990-10-19

Substantially Equivalent

Precise Optics

FDA 510(k) clearance K903457 for PRECISION OPTICS IMAGE BEAMSPLITTER (COUPLER), Substantially Equivalent on 1990-10-19. Applicant: Precise Optics. Device class: 2.

Clearance details

Applicant: Precise Optics
Product code: Code FET
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1990-08-01
Decision date: 1990-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gardner, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FET

product code FET

Injury: 313
Malfunction: 54,276
Total: 54,589

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.