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FDA 510(k)

LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA

K-Number: K001772 · 2000-07-06

ApplicantTaracan Pty. , Ltd.
Decision Date2000-07-06
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA is the device name listed in this FDA 510(k) record. The listed applicant is Taracan Pty. , Ltd.. It received FDA 510(k) clearance on 2000-07-06 under 510(k) number K001772. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA?

LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA is a medical device that received FDA 510(k) clearance on 2000-07-06. The listed applicant is Taracan Pty. , Ltd.. The 510(k) number is K001772.

When did LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA receive FDA 510(k) clearance?

LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA received FDA 510(k) clearance on 2000-07-06, under 510(k) number K001772.

Who is the listed applicant for LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA?

The FDA 510(k) record lists Taracan Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA?

The FDA product code for LASEREX ERA ARTICULATED ARM KIT, MODEL LQP4106-AA is HQF.

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Official Source

View on FDA Database →

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

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