Skytron, Div. the Kmw Group, Inc.
Skytron, Div. the Kmw Group, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2007, with 9 FDA device recalls on record.
Top product codes for Skytron, Div. the Kmw Group, Inc.
FDA recalls by Skytron, Div. the Kmw Group, Inc.
- Z-1309-2022 — Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
- Z-1861-2021 — Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32
- Z-0071-2021 — VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration Control System Model: VGDF-SKY (version 2). For communication and visual image management in the operating room suite.
- Z-0109-2021 — SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained video switching and control unit for use in the operating room.
- Z-1569-2020 — Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1
- Z-1779-2019 — Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and materials used in the health care industry
- Z-1844-2016 — EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide Operating Table General Purpose Surgical Table
- Z-1871-2016 — Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, single monitor mount, 27inch max. screen size
- Z-0655-2016 — Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment pendant / booms
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
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.