POSEY BED— 510(k) K103817

Name: FDA 510(k) clearance K103817
Creator: U.S. Food and Drug Administration
Published: 2011-04-22

Substantially Equivalent

J. T. Posey Co.

FDA 510(k) clearance K103817 for POSEY BED, Substantially Equivalent on 2011-04-22. Applicant: J. T. Posey Co.. Device class: 1.

Clearance details

Applicant: J. T. Posey Co.
Product code: Code OYS
Device class: Class 1
Regulation: 21 CFR 880.6760
Advisory panel: General Hospital
Date received: 2010-12-29
Decision date: 2011-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arcadia, CA, US

Download summary PDF View on FDA.gov ↗

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K113355 — POSEY BED2012-05-02
K113357 — POSEY BED2012-03-21

More clearances from J. T. Posey Co.

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K963410 — POSEY STRAIGHT JACKETS1996-11-22
K963414 — MULTIPLE BELTS1996-11-22
K963436 — RESTRAINT ACCESSORIES1996-11-22
K963442 — JACKETS AND VESTS1996-11-22
K963411 — POSEY LAPTOP TRAYS1996-11-19

Adverse events under product code OYS

product code OYS

Death: 3
Total: 3

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.