510(k) K771385
K771385 is an FDA 510(k) premarket notification submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic for the device "2 JET SET". The FDA issued a decision of Substantially Equivalent on August 4, 1977. The device falls under product code BYF (Mask, Oxygen, Low Concentration, Venturi), a Class I device regulated under 21 CFR 868.5600. Bd Becton Dickinson Vacutainer Systems Preanalytic has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 4, 1977
- Date Received
- July 27, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mask, Oxygen, Low Concentration, Venturi
- Device Class
- Class I
- Regulation Number
- 868.5600
- Review Panel
- AN
- Submission Type