510(k) K800296
K800296 is an FDA 510(k) premarket notification submitted by Dade, Baxter Travenol Diagnostics, Inc. for the device "WHOLE BLOOD GAS CONTROL, LEVELS 1,2,&3". The FDA issued a decision of Substantially Equivalent on March 5, 1980. The device falls under product code GGM (Control, Hemoglobin), a Class II device regulated under 21 CFR 864.8625. Dade, Baxter Travenol Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 5, 1980
- Date Received
- February 11, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Control, Hemoglobin
- Device Class
- Class II
- Regulation Number
- 864.8625
- Review Panel
- HE
- Submission Type