Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POSEY HUGGER

K-Number: K963409 · 1996-11-14

ApplicantJ. T. Posey Co.
Decision Date1996-11-14
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POSEY HUGGER is the device name listed in this FDA 510(k) record. The listed applicant is J. T. Posey Co.. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K963409. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSEY HUGGER?

POSEY HUGGER is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is J. T. Posey Co.. The 510(k) number is K963409.

When did POSEY HUGGER receive FDA 510(k) clearance?

POSEY HUGGER received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963409.

Who is the listed applicant for POSEY HUGGER?

The FDA 510(k) record lists J. T. Posey Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSEY HUGGER?

The FDA product code for POSEY HUGGER is FMQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing J. T. Posey Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113355POSEY BEDK113357POSEY BEDK103817POSEY BEDK963410POSEY STRAIGHT JACKETSK963414MULTIPLE BELTSK963436RESTRAINT ACCESSORIES

View all 13 devices →

Related Devices (Code: FMQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K110377PROTECTIVE RESTRAINTMedi-Tech Intl. Corp.K081264STATSTRAP NEONATAL INCUBATOR SAFETY STRAP, MODELS SS-001, SS-002Children'S Health First, Inc.K080448CENTURION PROTECTIVE RESTRAINT, SCR SERIESTri-State Hospital Supply Corp.K013239COMFORTCARE COMPRESSION SUPPORT WITH MAGNETS COMFORTCARE MAGNETIC INSOLESMed Gen, Inc.K010818INFANT LIMB HOLDER, MODELS 306080 & 306081Skil-Care Corp.K010644CINCH-TYPE DISPOSABLE LIMB HOLDERS, MODEL 912025Skil-Care Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑