| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the Original HDE to get an up-to-date view of this device. |
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| Trade Name | TAS ECT TEST |
| Classification Name | test, ecarin clotting time (ect) |
| Generic Name | test, ecarin clotting time (ect) |
| Applicant |
| Cardiovascular Diagnostics, Inc. |
| 9401 globe center dr.,suite |
| 140 |
| morrisville, NC 27560 |
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| HDE Number | H990012 |
| Supplement Number | S001 |
| Date Received | 02/05/2004 |
| Decision Date | 08/31/2004 |
| Product Code | |
| Advisory Committee |
Hematology |
| Supplement Type | normal 75 day track |
| Supplement Reason | location change - manufacturer/sterilizer/packager/supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Replacement of the knoll pharmaceuticals peg hirudin with refludan r-hirudin;an increase in lot release acceptance criteria, from precision of 8% to 10%cv, for clotting times of the ect test cards;removal of the in-process range of 180-190 seconds for target clotting times;replacement of the card calibration test procedure. |
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