FDA 510(k) Applications Submitted by JACK SPEER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040065 |
01/13/2004 |
JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES |
JACK SPEER AND ASSOC., INC. |
| K060352 |
02/13/2006 |
HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS |
HEALTH LINE INTERNATIONAL CORPORATION |
| K031189 |
04/15/2003 |
UUHC REPROCESSED COMPRESSION SLEEVE DEVICES |
UNIVERSITY OF UTAH HOSPITALS AND CLINICS |
| K031722 |
06/03/2003 |
JSA REPROCESSED COMPRESSION SLEEVE DEVICES |
JACK SPEER AND ASSOC., INC. |
| K012614 |
08/13/2001 |
KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
| K012624 |
08/13/2001 |
REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURS |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
| K012632 |
08/13/2001 |
TOURNIQUET CUFF; PNEUMATIC TOURNIQUET |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
| K012640 |
08/13/2001 |
ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
| K033615 |
11/17/2003 |
WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES |
WHEATON FRANCISCAN SERVICES INC., SUPPLY CHAIN |
| K974617 |
12/11/1997 |
PERIPHERAL VASCULAR DILATOR |
ENDOVASCULAR INSTRUMENTS, INC. |
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