510(k) K823142
K823142 is an FDA 510(k) premarket notification submitted by Seven Harvest Intl. Import & Export for the device "OXYGEN TUBINGS". The FDA issued a decision of Substantially Equivalent on November 29, 1982. The device falls under product code BYX (Tubing, Pressure And Accessories), a Class I device regulated under 21 CFR 868.5860. Seven Harvest Intl. Import & Export has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 29, 1982
- Date Received
- October 25, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubing, Pressure And Accessories
- Device Class
- Class I
- Regulation Number
- 868.5860
- Review Panel
- AN
- Submission Type