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.. Device class: 2.

Clearance details

Applicant: Retmap, Inc.
Product code: Code HLZ
Device class: Class 2
Regulation: 21 CFR 886.1220
Advisory panel: Ophthalmic
Date received: 2023-07-31
Decision date: 2023-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLZ

K253586 — RM Electrode (RMH 25-01)2026-04-01
K961805 — TOMEY DTL ELECTRODE1997-05-09
K926540 — SOPHER AND BIERER OVUM FORCEPS1994-02-25
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Data sourced from openFDA. This site is unofficial and independent of the FDA.