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FDA 510(k)

V-DELTA N (V-DELTA LOY), AUROFLUID 2PF

K-Number: K944572 · 1994-11-02

ApplicantMetalor
Decision Date1994-11-02
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

V-DELTA N (V-DELTA LOY), AUROFLUID 2PF is the device name listed in this FDA 510(k) record. The listed applicant is Metalor. It received FDA 510(k) clearance on 1994-11-02 under 510(k) number K944572. 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 V-DELTA N (V-DELTA LOY), AUROFLUID 2PF?

V-DELTA N (V-DELTA LOY), AUROFLUID 2PF is a medical device that received FDA 510(k) clearance on 1994-11-02. The listed applicant is Metalor. The 510(k) number is K944572.

When did V-DELTA N (V-DELTA LOY), AUROFLUID 2PF receive FDA 510(k) clearance?

V-DELTA N (V-DELTA LOY), AUROFLUID 2PF received FDA 510(k) clearance on 1994-11-02, under 510(k) number K944572.

Who is the listed applicant for V-DELTA N (V-DELTA LOY), AUROFLUID 2PF?

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

What is the FDA product code for V-DELTA N (V-DELTA LOY), AUROFLUID 2PF?

The FDA product code for V-DELTA N (V-DELTA LOY), AUROFLUID 2PF 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 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.

K935387PONTOR LFCK935388CERAPALL 4CF

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.

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