Skytron, Div. the Kmw Group, Inc.
FDA 510(k) medical device clearances.
Top product codes for Skytron, Div. the Kmw Group, Inc.
Recent clearances by Skytron, Div. the Kmw Group, Inc.
- K071698 — AURORA LED SERIES SURGICAL LIGHTS
- K021585 — STELLAR SERIES SURGICAL LIGHTS WITH HERMES
- K002463 — STELLAR
- K992090 — MILLENNIUM GOLD
- K950192 — SKYTRON SKYBOOM SERIES
- K940616 — SKYTRON ELITE 3500 TABLE
- K933564 — SKYTRON EXAM LIGHT
- K926045 — SKYTRON LIFE ISLAND 21
- K915285 — SKYTRON INFINITY SERIES SURGICAL LIGHTS
- K900472 — SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI
- K900211 — SKYTRON UNIVERSE SERIES SURGICAL LIGHTS
- K900290 — SKYTRON MODEL 1100 AND MODEL 142
- K873478 — SKYTRON MODEL 130 SURGICAL TABLE
- K870045 — SKYTRON MODEL 610-2
- K853480 — SKYTRON ELITE 6000 & 6001 SURGICAL TABLES
- K853479 — SKYTRON ELITE 300 SURGERY TABLE
- K851829 — SKYTRON ELITE 3100 SURGICAL TABLE
- K851830 — SKYTRON ELITE 7000 MICRO-SURGERY TABLE
- K811311 — SKYTRON ELITE SURGICAL TABLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.