510(k) K822466
K822466 is an FDA 510(k) premarket notification submitted by American Dade for the device "THROMBIN TIME TEST". The FDA issued a decision of Substantially Equivalent on September 14, 1982. The device falls under product code GJA (Test, Thrombin Time), a Class II device regulated under 21 CFR 864.7875. American Dade has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 14, 1982
- Date Received
- August 16, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Test, Thrombin Time
- Device Class
- Class II
- Regulation Number
- 864.7875
- Review Panel
- HE
- Submission Type