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Data / Medical devices / Bed-Patient Activity Monitoring System

Bed-Patient Activity Monitoring System (SBO): 3 FDA-registered makers in 1 country

3 establishments in 1 country are registered with the FDA to make Bed-Patient Activity Monitoring System (product code SBO, Class 1, 21 CFR 880.2400). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on June 21, 2024, and lists 0 recall events (0 Class I). FDA data exported November 3, 2026.

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Product code
SBO
Device class
1
Regulation
880.2400
Medical specialty
General Hospital

Makers by country

CountryMakers
United States3

Makers of Bed-Patient Activity Monitoring System

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Position Health, LLCLake Forest, IL, United StatesManufacturer, Specification developer1June 21, 2024000api.fda.gov
Aqp One, Inc.Garden Grove, CA, United StatesSpecification developer0000api.fda.gov
Praesidium IncSaint George, UT, United StatesManufacturer0000api.fda.gov

Updated June 21, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.