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FDA 510(k)

MONTGOMERY TRACHEAL T-TUBE

K-Number: K841266 · 1984-06-14

ApplicantE. Benson Hood Laboratories, Inc.
Decision Date1984-06-14
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONTGOMERY TRACHEAL T-TUBE is the device name listed in this FDA 510(k) record. The listed applicant is E. Benson Hood Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-14 under 510(k) number K841266. 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 MONTGOMERY TRACHEAL T-TUBE?

MONTGOMERY TRACHEAL T-TUBE is a medical device that received FDA 510(k) clearance on 1984-06-14. The listed applicant is E. Benson Hood Laboratories, Inc.. The 510(k) number is K841266.

When did MONTGOMERY TRACHEAL T-TUBE receive FDA 510(k) clearance?

MONTGOMERY TRACHEAL T-TUBE received FDA 510(k) clearance on 1984-06-14, under 510(k) number K841266.

Who is the listed applicant for MONTGOMERY TRACHEAL T-TUBE?

The FDA 510(k) record lists E. Benson Hood Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONTGOMERY TRACHEAL T-TUBE?

The FDA product code for MONTGOMERY TRACHEAL T-TUBE is BTO.

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Other records listing E. Benson Hood Laboratories, 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.

K983878CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPEK841350SALIVARY BYPASS TUBEK841349ESOPHAGEAL TUBEK841348UMBRELLA KEELK841347LARYNGEAL STENT

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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