FDA Device Intelligence
Home › NIHON KOHDEN AMERICA, INC. › PSG-1100

PSG-1100

NIHON KOHDEN AMERICA, INC. · Model PSG-1100 · UDI-DI 00841983103667

OLVGWQ Prescription
10
510(k) clearances
21
Adverse events
1
Recalls
48
Facilities

Description

POLYSOMONOGRAPHY AMPLIFIER KIT

Recalls

DateFirmReason
2018-02-01Natus Neurology IncPotential to be able to import an ambulatory exam for a patient for which the exam was not started.

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.