FDA 510(k) Applications Submitted by SKYLARK DEVICE CO., LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K964434 |
11/05/1996 |
SD-970EMS ELECTRICAL MUSCULAR STIMULATOR |
SKYLARK DEVICE CO., LTD. |
| K963729 |
09/16/1996 |
SD-610M(ALSO KNOWN AS STANDARD TENS, SD-609M,SD-611M, GLC-I STANDARD) |
SKYLARK DEVICE CO., LTD. |
| K983964 |
11/06/1998 |
BATCH #6060 CONDUCTIVE GEL |
SKYLARK DEVICE CO., LTD. |
| K981449 |
04/22/1998 |
SD-956 ULTRASOUND THERAPY |
SKYLARK DEVICE CO., LTD. |
| K984506 |
12/18/1998 |
SD-100 SKYEAR THERMOMETER |
SKYLARK DEVICE CO., LTD. |
| K964437 |
11/05/1996 |
GB-1002 TENS WITH MASSAGE |
SKYLARK DEVICE CO., LTD. |
| K990233 |
01/25/1999 |
ST-302 INFRAREX |
SKYLARK DEVICE CO., LTD. |
| K974585 |
12/08/1997 |
IF-727 INTERFERENTIAL STIMULATOR |
SKYLARK DEVICE CO., LTD. |
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