FDA 510(k)

STANDING FRAME

K-Number: K813025 · 1981-11-10

Decision Date1981-11-10

Product Code

DecisionSubstantially Equivalent

Device Summary

STANDING FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Barnett Medical. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K813025. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STANDING FRAME?

STANDING FRAME is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Barnett Medical. The 510(k) number is K813025.

When did STANDING FRAME receive FDA 510(k) clearance?

STANDING FRAME received FDA 510(k) clearance on 1981-11-10, under 510(k) number K813025.

Who is the listed applicant for STANDING FRAME?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Barnett Medical as applicant

K812903HUTT SWIVEL WALKER & HUTT STANDING FRAME

Official Source

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