TRACHEOSTOMY CARE KIT— 510(k) K855130
Substantially EquivalentDynarex Corp.
FDA 510(k) clearance K855130 for TRACHEOSTOMY CARE KIT, Substantially Equivalent on 1986-03-04. Applicant: Dynarex Corp.. Device class: 2.
Clearance details
- Applicant
- Dynarex Corp.
- Product code
- Code BTO
- Device class
- Class 2
- Regulation
- 21 CFR 868.5800
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Brewster, NY, US
Recent devices under product code BTO
view all- K253063 — Venti-Trach Tracheostomy Tube (4 models)
- K242921 — 5300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm +3 more
- K233713 — Pilling Tracheostomy Tubes
- K192511 — Venner 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 mm
- K173384 — BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube
More clearances from Dynarex Corp.
view all- K052743 — DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921
- K052314 — DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
- K012816 — DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
- K012957 — TOWEL DRAPE, MODELS 4409, 4410
- K012917 — DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
Adverse events under product code BTO
product code BTO- Death
- 14
- Injury
- 328
- Malfunction
- 1,851
- Total
- 2,193
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.