510(k) K913828
K913828 is an FDA 510(k) premarket notification submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic for the device "QTEST INFLUENZA A". The FDA issued a decision of Substantially Equivalent on September 23, 1991. The device falls under product code GNT (Antigens, Ha (Including Ha Control), Influenza Virus A, B, C), a Class I device regulated under 21 CFR 866.3330. Bd Becton Dickinson Vacutainer Systems Preanalytic has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 23, 1991
- Date Received
- August 26, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigens, Ha (Including Ha Control), Influenza Virus A, B, C
- Device Class
- Class I
- Regulation Number
- 866.3330
- Review Panel
- MI
- Submission Type