RM Electrode (RMH 23-01)— 510(k) K232273

Substantially Equivalent

Retmap, Inc.

FDA 510(k) clearance K232273 for RM Electrode (RMH 23-01), Substantially Equivalent on 2023-12-07. Applicant: Retmap, Inc..

Clearance details

Applicant: Retmap, Inc.
Product code: Code HLZ
Advisory panel: Ophthalmic
Date received: 2023-07-31
Decision date: 2023-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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