FDA 510(k) Applications Submitted by HUNTLEIGH HEALTHCARE, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K012008 |
06/27/2001 |
STS RANGE , MODELS STS20,STS30,STS40 |
HUNTLEIGH HEALTHCARE, INC. |
| K022786 |
08/22/2002 |
DVT60 |
HUNTLEIGH HEALTHCARE, INC. |
| K963711 |
09/16/1996 |
BABY DOPPLEX (3000) |
HUNTLEIGH HEALTHCARE, INC. |
| K984307 |
12/02/1998 |
MODIFICATION OF: RHEO DOPPLEX II |
HUNTLEIGH HEALTHCARE, INC. |
| K965153 |
12/23/1996 |
HUNTLEIGH FP5000 SYSTEM MODEL FP5000 |
HUNTLEIGH HEALTHCARE, INC. |
| K990569 |
02/23/1999 |
BABY DOPPLEX 4000, MODEL BD 4000 |
HUNTLEIGH HEALTHCARE, INC. |
| K001882 |
06/21/2000 |
BABY DOPPLEX 4002-TWINS, MODEL BD4002 |
HUNTLEIGH HEALTHCARE, INC. |
| K002186 |
07/20/2000 |
VASCULAR ASSIST |
HUNTLEIGH HEALTHCARE, INC. |
| K010744 |
03/13/2001 |
FLOWTRON UNIVERSAL, MODEL AC600 |
HUNTLEIGH HEALTHCARE, INC. |
| K010889 |
03/26/2001 |
BABY DOPPLEX 3000 MK 2 (BD3000) |
HUNTLEIGH HEALTHCARE, INC. |
| K010894 |
03/26/2001 |
BABY DOPPLEX 3002 (BD3002) |
HUNTLEIGH HEALTHCARE, INC. |
| K032315 |
07/28/2003 |
IOP8 INTRA OPERATIVE PROBE |
HUNTLEIGH HEALTHCARE, INC. |
|
|
