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FDA 510(k)

DOVER LOW PRESSURE TRACHEAL TUBE

K-Number: K761258 · 1976-12-23

ApplicantWill Ross Co.
Decision Date1976-12-23
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DOVER LOW PRESSURE TRACHEAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1976-12-23 under 510(k) number K761258. 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 DOVER LOW PRESSURE TRACHEAL TUBE?

DOVER LOW PRESSURE TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1976-12-23. The listed applicant is Will Ross Co.. The 510(k) number is K761258.

When did DOVER LOW PRESSURE TRACHEAL TUBE receive FDA 510(k) clearance?

DOVER LOW PRESSURE TRACHEAL TUBE received FDA 510(k) clearance on 1976-12-23, under 510(k) number K761258.

Who is the listed applicant for DOVER LOW PRESSURE TRACHEAL TUBE?

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

What is the FDA product code for DOVER LOW PRESSURE TRACHEAL TUBE?

The FDA product code for DOVER LOW PRESSURE TRACHEAL TUBE is BTO.

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Other records listing Will Ross 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.

K780850SEARLE NEONATAL OXYGEN PROBEK771561DOVER URINE METERK771132KENWOOD BIOLOGICAL STEOILIZ. INDICATORK770608WALKING AIDK770609TABLE, MASSAGE & TREATMHNT, FIXED HEIGHTK770607TRACTION HARNESS

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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

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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