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)

MURPHY ADJUSTABLE SPLINT

K-Number: K854270 · 1985-12-09

ApplicantComfortex, Inc.
Decision Date1985-12-09
Product CodeKQZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MURPHY ADJUSTABLE SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Comfortex, Inc.. It received FDA 510(k) clearance on 1985-12-09 under 510(k) number K854270. The device is classified under product code KQZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MURPHY ADJUSTABLE SPLINT?

MURPHY ADJUSTABLE SPLINT is a medical device that received FDA 510(k) clearance on 1985-12-09. The listed applicant is Comfortex, Inc.. The 510(k) number is K854270.

When did MURPHY ADJUSTABLE SPLINT receive FDA 510(k) clearance?

MURPHY ADJUSTABLE SPLINT received FDA 510(k) clearance on 1985-12-09, under 510(k) number K854270.

Who is the listed applicant for MURPHY ADJUSTABLE SPLINT?

The FDA 510(k) record lists Comfortex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MURPHY ADJUSTABLE SPLINT?

The FDA product code for MURPHY ADJUSTABLE SPLINT is KQZ.

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 Comfortex, Inc. 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.

K860037SUSPENDER ORTHOPEDIC SUSPENSION DEVICEK855179TRANSFER-TRAX (TM) SPLINT TRACTIONK855181COMFORTEX WHEELCHAIR CUSHION

Related Devices (Code: KQZ)

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.

K884132TECNOL BUCKS TRACTION W/HEEL PROTECTORTechnol, Inc.K882640TECNOL SECURE-ALL PELVIC TRACTION BELTTecnol New Jersey Wound Care, Inc.K871900OVER DRAPE LEG HOLDERAvec Scientific Design Corp.K871296T.E.D.(TM) TRACTION DEVICEThe Kendal Co.K831002TPG 1000Physical Diagnostics, Inc.K823660UNIVERSAL BUCKS TRACTIONWarm & Form, Orthopedic Materials

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.

↑