Skylark Device Co., Ltd.
Skylark Device Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1999.
Top product codes for Skylark Device Co., Ltd.
Recent clearances by Skylark Device Co., Ltd.
- K990233 — ST-302 INFRAREX
- K984506 — SD-100 SKYEAR THERMOMETER
- K981449 — SD-956 ULTRASOUND THERAPY
- K983964 — BATCH #6060 CONDUCTIVE GEL
- K964437 — GB-1002 TENS WITH MASSAGE
- K974585 — IF-727 INTERFERENTIAL STIMULATOR
- K964434 — SD-970EMS ELECTRICAL MUSCULAR STIMULATOR
- K963729 — SD-610M(ALSO KNOWN AS STANDARD TENS, SD-609M,SD-611M, GLC-I STANDARD)
- K946337 — IT-727 (ALSO KNOWN AS IT-610, IT-600 AND DYNAPHOR II
- K946299 — PGS123 AND HVS-123
- K934051 — BIO SDP (AKA SATURN SD, GLC-III SD & STAT-SD)
- K930535 — IF400
- K931079 — STAT-TENS
- K925729 — SD-602 SD MODE 11, SD-603 SD MOD 111
- K923934 — TX-3 SD
- K923935 — SD-605 SD II PROGRAM
- K923298 — MICRO 100,200,300, & 400 TENS
- K912643 — ELECTRODE
- K912642 — EMS300, EMS400, EMS8000
- K912178 — BIO TENS 601, 606 AND 608 (3000)
Data sourced from openFDA. This site is unofficial and independent of the FDA.