EndoSign® Cell collection device (ES-CYT-102)— 510(k) K233142

Name: FDA 510(k) clearance K233142
Creator: U.S. Food and Drug Administration
Published: 2024-01-19

Substantially Equivalent

Cyted Limited

FDA 510(k) clearance K233142 for EndoSign® Cell collection device (ES-CYT-102), Substantially Equivalent on 2024-01-19. Applicant: Cyted Limited. Device class: 2.

Clearance details

Applicant: Cyted Limited
Product code: Code EOX
Device class: Class 2
Regulation: 21 CFR 874.4710
Advisory panel: Ear, Nose, Throat
Date received: 2023-09-27
Decision date: 2024-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, GB

Download summary PDF View on FDA.gov ↗

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