Amber Mill Q Series & Amber Mill Direct Series— 510(k) K202952

Name: FDA 510(k) clearance K202952
Creator: U.S. Food and Drug Administration
Published: 2021-08-26

Substantially Equivalent

Hass Corp.

FDA 510(k) clearance K202952 for Amber Mill Q Series & Amber Mill Direct Series, Substantially Equivalent on 2021-08-26. Applicant: Hass Corp.. Device class: 2.

Clearance details

Applicant: Hass Corp.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2020-09-30
Decision date: 2021-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gangneung-Si, KR

Download summary PDF View on FDA.gov ↗

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More clearances from Hass Corp.

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K260859 — Rosetta SM, Rosetta SP2026-06-11
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K111573 — MONOBLOC BM SERIES2011-08-26
K102305 — HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P2010-12-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.