510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K170183Substantially Equivalent

Cetus system, Cetus probe

A.R.C. Laser GmbH, Nurnberg, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170183 is the FDA 510(k) clearance record for Cetus system, Cetus probe, a class II device, cleared for A.R.C Laser GmbH on under FDA product code HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered). FDA records list 10 510(k) clearances for A.R.C Laser GmbH, from to . As of , FDA records show no recalls naming K170183.

Clearance record

Decision date
Received
(247 days to decision)
Product code
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Regulation
21 CFR 886.4150
Device class
Class II
Review panel
Ophthalmic
Applicant
A.R.C Laser GmbH Bessemer St.14, Nurnberg, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HQE

Trailing 12 months

FDA records hold no clearances under product code HQE in the trailing twelve months.

FDA records show no clearances under product code HQE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HQE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260