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FDA 510(k)

TEFGEN-FD

K-Number: K935137 · 1994-08-15

ApplicantAmerican Custom Medical, Inc.
Decision Date1994-08-15
Product CodeNPK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEFGEN-FD is the device name listed in this FDA 510(k) record. The listed applicant is American Custom Medical, Inc.. It received FDA 510(k) clearance on 1994-08-15 under 510(k) number K935137. The device is classified under product code NPK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEFGEN-FD?

TEFGEN-FD is a medical device that received FDA 510(k) clearance on 1994-08-15. The listed applicant is American Custom Medical, Inc.. The 510(k) number is K935137.

When did TEFGEN-FD receive FDA 510(k) clearance?

TEFGEN-FD received FDA 510(k) clearance on 1994-08-15, under 510(k) number K935137.

Who is the listed applicant for TEFGEN-FD?

The FDA 510(k) record lists American Custom Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEFGEN-FD?

The FDA product code for TEFGEN-FD is NPK.

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 American Custom Medical, Inc. 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.

K965205TEFGEN - LSK964656TEFGEN GUIDED TISSUE MEMBRANEK944413ACM PTFE SURGICAL MESHK933800FLUOROFILM(R)

Related Devices (Code: NPK)

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.

K221851Lumina-PTFE TitaniumCriteria Industria E Comercio DE Produtos MedicinaisK222549OpenTexPurgo Biologics, Inc.K211554InnoGenic Non-resorbable MembraneCowellmedi Co., Ltd.K210797Bio-MEM Ti Reinforced MembraneB&Medi Co., Ltd.K201187Cytoplast Titanium-Reinforced PTFE MembranesOsteogenics Biomedical, Inc.K171774RPM Reinforced PTFE MeshOsteogenics Biomedical, Inc.

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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