FDA Device Intelligence
HomeSKYTRON LLC › Transfer board

Transfer board

SKYTRON LLC · Model 4-030-18 · UDI-DI 10841736112660

LWG Prescription
4
510(k) clearances
36
Adverse events
1
Recalls
59
Facilities

Description

Transfer board, side rail type (3100A, 6002, 1700, 6700 SERIES & 3600B)

Recalls

DateFirmReason
2016-04-19Berchtold Corp.The Surgical Table Cushion (HybriGel Pads) could potentially contain staples that's secure two underlying fabrics, which would be captured on certain scans on patients, such as x-r

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.