MONOJECT SAMPLETTE SEPARATOR TUBE— 510(k) K941291
Substantially EquivalentSherwood Medical Co.
FDA 510(k) clearance K941291 for MONOJECT SAMPLETTE SEPARATOR TUBE, Substantially Equivalent on 1994-10-27. Applicant: Sherwood Medical Co.. Device class: 1.
Clearance details
- Applicant
- Sherwood Medical Co.
- Product code
- Code GIO
- Device class
- Class 1
- Regulation
- 21 CFR 864.6150
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St.Louis, MO, US
Recent devices under product code GIO
view allMore clearances from Sherwood Medical Co.
view all- K981365 — MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS
- K960982 — MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULA
- K962880 — SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEM
- K960574 — ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEM
- K960677 — KANGAROO JEJUNAL FEEDING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.