Cleared Traditional

EL27-Compact; Sterile EHL-Probes

K230488 · Walz Elektronik GmbH · Gastroenterology & Urology
Aug 2023
Decision
189d
Days
Class 2
Risk

About This 510(k) Submission

K230488 is an FDA 510(k) clearance for the EL27-Compact; Sterile EHL-Probes, a Lithotriptor, Electro-hydraulic (Class II — Special Controls, product code FFK), submitted by Walz Elektronik GmbH (Rohrdorf, DE). The FDA issued a Cleared decision on August 31, 2023, 189 days after receiving the submission on February 23, 2023. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4480.

Submission Details

510(k) Number K230488 FDA.gov
FDA Decision Cleared SESE
Date Received February 23, 2023
Decision Date August 31, 2023
Days to Decision 189 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FFK — Lithotriptor, Electro-hydraulic
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.4480

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