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FDA 510(k)

LARKEL DEVICE W/ATTACHMENTS A-H

K-Number: K872486 · 1987-09-16

ApplicantSeidel Medizin GmbH
Decision Date1987-09-16
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARKEL DEVICE W/ATTACHMENTS A-H is the device name listed in this FDA 510(k) record. The listed applicant is Seidel Medizin GmbH. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K872486. 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 LARKEL DEVICE W/ATTACHMENTS A-H?

LARKEL DEVICE W/ATTACHMENTS A-H is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Seidel Medizin GmbH. The 510(k) number is K872486.

When did LARKEL DEVICE W/ATTACHMENTS A-H receive FDA 510(k) clearance?

LARKEL DEVICE W/ATTACHMENTS A-H received FDA 510(k) clearance on 1987-09-16, under 510(k) number K872486.

Who is the listed applicant for LARKEL DEVICE W/ATTACHMENTS A-H?

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

What is the FDA product code for LARKEL DEVICE W/ATTACHMENTS A-H?

The FDA product code for LARKEL DEVICE W/ATTACHMENTS A-H 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 Seidel Medizin GmbH 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.

K953559LARKEL DEVICE WITH ATTACHMENTS A-H(MODIFICATION)

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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