FDA 510(k)

LION Photocoagulator

K-Number: K201623 · 2020-08-11

Decision Date2020-08-11

Product CodeHQF

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

LION Photocoagulator is the device name listed in this FDA 510(k) record. The listed applicant is Norlase Aps. It received FDA 510(k) clearance on 2020-08-11 under 510(k) number K201623. 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 LION Photocoagulator?

LION Photocoagulator is a medical device that received FDA 510(k) clearance on 2020-08-11. The listed applicant is Norlase Aps. The 510(k) number is K201623.

When did LION Photocoagulator receive FDA 510(k) clearance?

LION Photocoagulator received FDA 510(k) clearance on 2020-08-11, under 510(k) number K201623.

Who is the listed applicant for LION Photocoagulator?

The FDA 510(k) record lists Norlase Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LION Photocoagulator?

The FDA product code for LION Photocoagulator is HQF.

Other records listing Norlase Aps as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242397LYNX Photocoagulator K190083Leaf Photocoagulator

Related Devices (Code: HQF)

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel Medical K251772Navilas Laser System 577sl (156691)Od-Os GmbH K243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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.