FDA 510(k) Applications Submitted by PROTEK MEDICAL PRODUCTS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K970885 |
03/11/1997 |
ULTRASOUND SYSTEMS DRAPE |
PROTEK MEDICAL PRODUCTS, INC. |
| K970889 |
03/11/1997 |
ULTRASOUND TRANSDUCER DRAPE |
PROTEK MEDICAL PRODUCTS, INC. |
| K970891 |
03/11/1997 |
DRAPE, SURGICAL-LATEX |
PROTEK MEDICAL PRODUCTS, INC. |
| K970893 |
03/11/1997 |
ULTRASOUND TRANSDUCER DRAPE |
PROTEK MEDICAL PRODUCTS, INC. |
| K971115 |
03/27/1997 |
GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE |
PROTEK MEDICAL PRODUCTS, INC. |
| K971722 |
05/09/1997 |
TRANS VAGINAL NEEDLE GUIDE |
PROTEK MEDICAL PRODUCTS, INC. |
| K973362 |
09/08/1997 |
NEEDLE GUIDE/GRID |
PROTEK MEDICAL PRODUCTS, INC. |
| K973622 |
09/23/1997 |
TRANSDUCER POSITIONER |
PROTEK MEDICAL PRODUCTS, INC. |
| K973958 |
10/16/1997 |
GENERAL PURPOSE ATL NEEDLE GUIDE KIT |
PROTEK MEDICAL PRODUCTS, INC. |
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