VENTRE/SPEC ALLERGEN CONTROL-INHALANT— 510(k) K820978
Substantially EquivalentVentrex Laboratories, Inc.
FDA 510(k) clearance K820978 for VENTRE/SPEC ALLERGEN CONTROL-INHALANT, Substantially Equivalent on 1982-06-11. Applicant: Ventrex Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventrex Laboratories, Inc.
- Product code
- Code DGC
- Device class
- Class 2
- Regulation
- 21 CFR 866.5510
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code DGC
view all- K231151 — Kenota 1 Total IgE; Kenota 1 (instrument)
- K214068 — Quantia IgE
- K220178 — Total Immunoglobulin E (IgE)
- K193493 — ADVIA Centaur Total IgE (tIgE)
- K161899 — ImmunoCAP Total IgE Calibrator Strip/Total IgE Curve Control Strip, ImmunoCAP Total IgE Calibrators/Total IgE Curve Controls, ImmunoCAP Specific IgE Calibrator Strip/Specific IgE Curve Control Strip, ImmunoCAP Specific IgE Calibrators/Specific IgE Curve Controls
More clearances from Ventrex Laboratories, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.