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FDA 510(k)

TODD MEDICAL/SKILLED CARE PRODUCTS

K-Number: K873499 · 1987-11-24

ApplicantTodd Medical, Inc.
Decision Date1987-11-24
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TODD MEDICAL/SKILLED CARE PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Todd Medical, Inc.. It received FDA 510(k) clearance on 1987-11-24 under 510(k) number K873499. 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 TODD MEDICAL/SKILLED CARE PRODUCTS?

TODD MEDICAL/SKILLED CARE PRODUCTS is a medical device that received FDA 510(k) clearance on 1987-11-24. The listed applicant is Todd Medical, Inc.. The 510(k) number is K873499.

When did TODD MEDICAL/SKILLED CARE PRODUCTS receive FDA 510(k) clearance?

TODD MEDICAL/SKILLED CARE PRODUCTS received FDA 510(k) clearance on 1987-11-24, under 510(k) number K873499.

Who is the listed applicant for TODD MEDICAL/SKILLED CARE PRODUCTS?

The FDA 510(k) record lists Todd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TODD MEDICAL/SKILLED CARE PRODUCTS?

The FDA product code for TODD MEDICAL/SKILLED CARE PRODUCTS 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 Todd Medical, 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.

K873288CLOSED FOLEY CATHETER SYSTEMK873287IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE)K873469TODD MEDICAL/SKILLED CARE PRODUCTSK850646ECLIPSE SELF ADHERING ELECTRODEK850004TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEF

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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