ClearanceBrief
510(k) K183231 ยท LNH System, Nuclear Magnetic Resonance Imaging

SIGNA Premier

ApplicantGe Medical Systems, LLC, Waukesha WI, US
DecisionSubstantially Equivalent, Jan 18, 2019
ReceivedNov 20, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183231

DateFirm and productCodeLinked 510(k)
Apr 2, 2026GE Healthcare LLC
SIGNA Premier systems
Open, Classified
LNHNone listed
Aug 13, 2025GE Medical Systems, LLC
GE SIGNA Premier, Nuclear Magnetic Resonance Imaging System
Open, Classified
LNHNone listed
Aug 2, 2024GE Medical Systems, LLC
SIGNA Premier, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
Open, Classified
LNHNone listed
Jun 24, 2022GE Healthcare, LLC
SIGNA Premier magnetic resonance scanner, model 5748519.
Open, Classified
LNHNone listed
Dec 23, 2021GE Healthcare, LLC
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclear magnetic resonance imaging system.
Open, Classified
LNHNone listed
Oct 16, 2021GE Healthcare, LLC
SIGNA Premier nuclear magnetic resonance imaging system
Terminated
LNHNone listed
Jul 12, 2021GE Healthcare, LLC
SIGNA Premier - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Open, Classified
LNHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.