510(k) K904639
K904639 is an FDA 510(k) premarket notification submitted by Pacific Consolidated Industries for the device "GENOX MODEL CT-1". The FDA issued a decision of Substantially Equivalent on Aug 13, 1991. The device falls under product code CAW (Generator, Oxygen, Portable), a Class II device regulated under 21 CFR 868.5440. Pacific Consolidated Industries has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 13, 1991
- Date Received
- Oct 11, 1990
- 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
- 510(k)