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)

THE FREEDOM BED

K-Number: K954671 · 1996-04-01

ApplicantProbed Medical Technologies, Inc.
Decision Date1996-04-01
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE FREEDOM BED is the device name listed in this FDA 510(k) record. The listed applicant is Probed Medical Technologies, Inc.. It received FDA 510(k) clearance on 1996-04-01 under 510(k) number K954671. The device is classified under product code IKZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE FREEDOM BED?

THE FREEDOM BED is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Probed Medical Technologies, Inc.. The 510(k) number is K954671.

When did THE FREEDOM BED receive FDA 510(k) clearance?

THE FREEDOM BED received FDA 510(k) clearance on 1996-04-01, under 510(k) number K954671.

Who is the listed applicant for THE FREEDOM BED?

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

What is the FDA product code for THE FREEDOM BED?

The FDA product code for THE FREEDOM BED is IKZ.

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

Related Devices (Code: IKZ)

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.

K972486PRESSUREGUARD IVSpan-America Medical Systems, Inc.K972111RUMORS DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K962788CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMGaymar Industries, Inc.K950756PULMONEX DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K950681MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPYInvacare Corp.K933964THE CRADLEThe Primal Energy Research Foundation

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.

↑