510(k) K802426
K802426 is an FDA 510(k) premarket notification submitted by Mada Medical Products, Inc. for the device "RESPO2 OXYGEN CONCENTRATOR". The FDA issued a decision of Substantially Equivalent on October 23, 1980. The device falls under product code CAW (Generator, Oxygen, Portable), a Class II device regulated under 21 CFR 868.5440. Mada Medical Products, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 23, 1980
- Date Received
- October 6, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Generator, Oxygen, Portable
- Device Class
- Class II
- Regulation Number
- 868.5440
- Review Panel
- AN
- Submission Type