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FDA 510(k)

HANAULUX 2005 SURGICAL LIGHT

K-Number: K932451 · 1993-11-12

ApplicantHeraeus Instruments GmbH
Decision Date1993-11-12
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HANAULUX 2005 SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus Instruments GmbH. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K932451. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANAULUX 2005 SURGICAL LIGHT?

HANAULUX 2005 SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Heraeus Instruments GmbH. The 510(k) number is K932451.

When did HANAULUX 2005 SURGICAL LIGHT receive FDA 510(k) clearance?

HANAULUX 2005 SURGICAL LIGHT received FDA 510(k) clearance on 1993-11-12, under 510(k) number K932451.

Who is the listed applicant for HANAULUX 2005 SURGICAL LIGHT?

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

What is the FDA product code for HANAULUX 2005 SURGICAL LIGHT?

The FDA product code for HANAULUX 2005 SURGICAL LIGHT is FTD.

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Related Devices (Code: FTD)

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.

K133425SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHTEngineered Medical Solutions Co., LLCK130513VOLISTA 400; VOLISTA 600Maquet S.A.S.K123776POLARIS 100/200Drager Medical GmbHK111020ATRICURE DISSECTORAtriCure, Inc.K100234HM-LAMP IIHillusa, Inc.K100884STRYKER KNIFELIGHTHowmedica Osteonics Corp.

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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