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FDA 510(k)

EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO-

K-Number: K830509 · 1983-03-29

ApplicantFrederic J. Toye, M.D.
Decision Date1983-03-29
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO- is the device name listed in this FDA 510(k) record. The listed applicant is Frederic J. Toye, M.D.. It received FDA 510(k) clearance on 1983-03-29 under 510(k) number K830509. 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 EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO-?

EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO- is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Frederic J. Toye, M.D.. The 510(k) number is K830509.

When did EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO- receive FDA 510(k) clearance?

EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO- received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830509.

Who is the listed applicant for EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO-?

The FDA 510(k) record lists Frederic J. Toye, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO-?

The FDA product code for EMERGENCY TRACHEOSTOMY & CRICOTHYROIDO- is BTO.

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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 Frederic J. Toye, M.D. 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.

K871199MODIFIED PERTRACH DISP. PEDIATRIC PERCUT. TRACHEO.K822440PERCUTANEOUS CRICOTHYROIDOTOMYK832498PERCUTANEOUS TRACHEOSTOMY DEVICEK821821PERCUTANEOUS TRACHEOSTOMY DEVICEK801379CUFFED TRACHEA TUBE FOR USE W/PERTRACH

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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