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FDA 510(k)

E-TENG MODEL EOR 1

K-Number: K122562 · 2013-08-09

ApplicantE-Teng Technology, Inc.
Decision Date2013-08-09
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

E-TENG MODEL EOR 1 is the device name listed in this FDA 510(k) record. The listed applicant is E-Teng Technology, Inc.. It received FDA 510(k) clearance on 2013-08-09 under 510(k) number K122562. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-TENG MODEL EOR 1?

E-TENG MODEL EOR 1 is a medical device that received FDA 510(k) clearance on 2013-08-09. The listed applicant is E-Teng Technology, Inc.. The 510(k) number is K122562.

When did E-TENG MODEL EOR 1 receive FDA 510(k) clearance?

E-TENG MODEL EOR 1 received FDA 510(k) clearance on 2013-08-09, under 510(k) number K122562.

Who is the listed applicant for E-TENG MODEL EOR 1?

The FDA 510(k) record lists E-Teng Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-TENG MODEL EOR 1?

The FDA product code for E-TENG MODEL EOR 1 is IPL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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