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FDA 510(k)

TRAUMAFUSE TRACH SHIELD

K-Number: K895162 · 1990-01-09

ApplicantThe Traumafuse Co.
Decision Date1990-01-09
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRAUMAFUSE TRACH SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is The Traumafuse Co.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K895162. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAUMAFUSE TRACH SHIELD?

TRAUMAFUSE TRACH SHIELD is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is The Traumafuse Co.. The 510(k) number is K895162.

When did TRAUMAFUSE TRACH SHIELD receive FDA 510(k) clearance?

TRAUMAFUSE TRACH SHIELD received FDA 510(k) clearance on 1990-01-09, under 510(k) number K895162.

Who is the listed applicant for TRAUMAFUSE TRACH SHIELD?

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

What is the FDA product code for TRAUMAFUSE TRACH SHIELD?

The FDA product code for TRAUMAFUSE TRACH SHIELD is BTO.

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.

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Other records listing The Traumafuse Co. 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.

K894721TRAUMAFUSE PERFUSION PRESSURE RELIEF VALVEK895132CONNELL-STEPHENS ENDO ANESS TUBEK890077TRAUMAFUSE RAPID INFUSION DEVICE

Related Devices (Code: BTO)

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.

K253063Venti-Trach Tracheostomy Tube (570 Series); Venti-Trach Tracheostomy Tube (571 Series); Venti-Trach Tracheostomy Tube (580 Series); Venti-Trach Tracheostomy Tube (581 Series)Vitaltec CorporationK2429215300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm; 5310600-5311000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, Fenestrated, sizes 6.0-10.0mm; 5400600-5401000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, sizes 6.0-10.0mm; 5410500-5411000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, Fenestrated, sizes 6.0-10.0mmVitaltec CorporationK233713Pilling Tracheostomy TubesTeleflex MedicalK192511Venner PneuX™ TT (Tracheostomy Tube) Size 7.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 8.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 9.0 mmVenner Medical (Singapore) Pte, Ltd.K173384BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tubeSmiths Medical Ads, Inc.K120079PRIMED TRACHEOSTOMY TUBES (MULTIPLE)Primed Halberstadt Medizintechnik GmbH

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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