| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device. |
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| Trade Name | VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR |
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| Classification Name | implantable cardioverter defibrillator (non-crt) |
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| Applicant | CARDIAC PACEMAKERS, INC. |
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| PMA Number | P910077 |
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| Supplement Number | S001 |
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| Date Received | 08/05/1994 |
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| Decision Date | 11/23/1994 |
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| Product Code | |
| Advisory Committee |
Anesthesiology |
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| Supplement Type | normal 180 day track |
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| Supplement Reason | location change - other |
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| Expedited Review Granted? | No |
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| Combination Product |
No
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