Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ILED

K-Number: K061317 · 2006-06-22

ApplicantTrumpf Kreuzer Medizin Systeme GmbH + Co.Kg
Decision Date2006-06-22
Product CodeFSY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ILED is the device name listed in this FDA 510(k) record. The listed applicant is Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg. It received FDA 510(k) clearance on 2006-06-22 under 510(k) number K061317. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILED?

ILED is a medical device that received FDA 510(k) clearance on 2006-06-22. The listed applicant is Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg. The 510(k) number is K061317.

When did ILED receive FDA 510(k) clearance?

ILED received FDA 510(k) clearance on 2006-06-22, under 510(k) number K061317.

Who is the listed applicant for ILED?

The FDA 510(k) record lists Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ILED?

The FDA product code for ILED is FSY.

Other records listing Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg 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.

K102758TRULIGHT 5520 AND TRULIGHT 5320

Related Devices (Code: FSY)

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.

K132747VISUM BLADE LED SURGICAL LIGHTING SYSTEMStryker CommunicationsK132307VIDA LED SURGICAL LIGHTING SYSTEMConvida Healthcare & Systems CorporationK131893AMICO CE SERIES SURGICAL LIGHTS, MIRA LED SERIES MINOR SURGICAL LIGHTSAjw Technology Consultants, Inc.K122875ORICARE L2700Oricare, Inc.K120392CHROMOPHARE F 628 AND F 528Berchtold GmbH & Co. KGK102758TRULIGHT 5520 AND TRULIGHT 5320Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg

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.

↑