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)

YELLOW SPECIAL

K-Number: K013506 · 2002-01-03

ApplicantMetalor Technologies USA
Decision Date2002-01-03
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

YELLOW SPECIAL is the device name listed in this FDA 510(k) record. The listed applicant is Metalor Technologies USA. It received FDA 510(k) clearance on 2002-01-03 under 510(k) number K013506. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YELLOW SPECIAL?

YELLOW SPECIAL is a medical device that received FDA 510(k) clearance on 2002-01-03. The listed applicant is Metalor Technologies USA. The 510(k) number is K013506.

When did YELLOW SPECIAL receive FDA 510(k) clearance?

YELLOW SPECIAL received FDA 510(k) clearance on 2002-01-03, under 510(k) number K013506.

Who is the listed applicant for YELLOW SPECIAL?

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

What is the FDA product code for YELLOW SPECIAL?

The FDA product code for YELLOW SPECIAL is EJT.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Metalor Technologies USA 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.

K020062XERAFITK013769V-GNATHOS SUPRAK013505AUROFLUID PLUS

Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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.

↑