MULTIPLE BELTS— 510(k) K963414

Name: FDA 510(k) clearance K963414
Creator: U.S. Food and Drug Administration
Published: 1996-11-22

Substantially Equivalent

J. T. Posey Co.

FDA 510(k) clearance K963414 for MULTIPLE BELTS, Substantially Equivalent on 1996-11-22. Applicant: J. T. Posey Co.. Device class: 1.

Clearance details

Applicant: J. T. Posey Co.
Product code: Code FMQ
Device class: Class 1
Regulation: 21 CFR 880.6760
Advisory panel: General Hospital
Date received: 1996-08-30
Decision date: 1996-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arcadia, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FMQ

view all

K110377 — PROTECTIVE RESTRAINT2011-04-25
K081264 — STATSTRAP NEONATAL INCUBATOR SAFETY STRAP, MODELS SS-001, SS-0022009-02-13
K080448 — CENTURION PROTECTIVE RESTRAINT, SCR SERIES2008-08-28
K013239 — COMFORTCARE COMPRESSION SUPPORT WITH MAGNETS COMFORTCARE MAGNETIC INSOLES2001-11-20
K010818 — INFANT LIMB HOLDER, MODELS 306080 & 3060812001-05-24

More clearances from J. T. Posey Co.

view all

K113355 — POSEY BED2012-05-02
K113357 — POSEY BED2012-03-21
K103817 — POSEY BED2011-04-22
K963410 — POSEY STRAIGHT JACKETS1996-11-22
K963436 — RESTRAINT ACCESSORIES1996-11-22

Adverse events under product code FMQ

product code FMQ

Death: 8
Total: 8

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.