Skylark Device Co., Ltd.
FDA 510(k) medical device clearances.
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.