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FDA 510(k)

TECHFIL

K-Number: K954801 · 1996-01-25

ApplicantTechnimeca Medic, Inc.
Decision Date1996-01-25
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TECHFIL is the device name listed in this FDA 510(k) record. The listed applicant is Technimeca Medic, Inc.. It received FDA 510(k) clearance on 1996-01-25 under 510(k) number K954801. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHFIL?

TECHFIL is a medical device that received FDA 510(k) clearance on 1996-01-25. The listed applicant is Technimeca Medic, Inc.. The 510(k) number is K954801.

When did TECHFIL receive FDA 510(k) clearance?

TECHFIL received FDA 510(k) clearance on 1996-01-25, under 510(k) number K954801.

Who is the listed applicant for TECHFIL?

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

What is the FDA product code for TECHFIL?

The FDA product code for TECHFIL is CAD.

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 Technimeca Medic, 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.

K953748TECHNOFIL

Related Devices (Code: CAD)

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.

K240375V80 Anesthetic Vaporizer (V80)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K172702Tec 820, Tec 850Datex-Ohmeda, Inc.K110608SEVOFLURANE VAPORIZER ADAPTORPiramal Critcal Care, Inc (Formerly Minrad, Inc)K060331SIGMA ALPHA VAPORIZERPenlon LimitedK053564KEYED FILLER BOTTLE ADAPTOR, MODELS 53450, 53452, 53453, 53454Penlon LimitedK051666GAV - GENERAL ANAESTHETIC VAPORIZERGeneral Anaesthetic Services Limited

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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