CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA— 510(k) K982269
Substantially EquivalentAllegiance Healthcare Corp.
FDA 510(k) clearance K982269 for CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA, Substantially Equivalent on 1998-07-23. Applicant: Allegiance Healthcare Corp.. Device class: 2.
Clearance details
- Applicant
- Allegiance Healthcare Corp.
- Product code
- Code MIA
- Device class
- Class 2
- Regulation
- 21 CFR 868.5150
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mcgraw Park, IL, US
Recent devices under product code MIA
view all- K172800 — Portex® Lancet Point Spinal Needles with NRFit connectors, Portex® Pencil Point Spinal Needles with NRFit connectors
- K051860 — FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837
- K983858 — SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES
- K971645 — REGANES SPINAL NEEDLE (VARIOUS)
- K970997 — NEO-CARE LUMBER PUNCTURE KIT
More clearances from Allegiance Healthcare Corp.
view all- K023673 — AIRLIFE DEMAND NASAL CANNULA
- K023419 — TRILAMINATE DRAPES/TIBURON
- K024120 — MODIFICATION TO TEMNO BIOPSY NEEDLES
- K024292 — MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIM
- K024102 — DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM
Data sourced from openFDA. This site is unofficial and independent of the FDA.