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)

SETUP WALKER ADJUSTABLE

K-Number: K772269 · 1977-12-20

ApplicantMed Fusion Systems, Inc.
Decision Date1977-12-20
Product CodeITQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SETUP WALKER ADJUSTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Med Fusion Systems, Inc.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772269. The device is classified under product code ITQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SETUP WALKER ADJUSTABLE?

SETUP WALKER ADJUSTABLE is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K772269.

When did SETUP WALKER ADJUSTABLE receive FDA 510(k) clearance?

SETUP WALKER ADJUSTABLE received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772269.

Who is the listed applicant for SETUP WALKER ADJUSTABLE?

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

What is the FDA product code for SETUP WALKER ADJUSTABLE?

The FDA product code for SETUP WALKER ADJUSTABLE is ITQ.

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 Med Fusion Systems, 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.

K873961INFUMED 300 AMBULATORY INFUSION PUMPK870524AMBULATORY INFUSION PUMP DRUG RESERVOIRK870907INTRODUCER, PERCUTANEOUSK864407REFILLABLE SYRINGEK863814BAG SPIKE EXTENSION SETK860616VOLUME CONTROL SET WITH EXTENSION

View all 22 devices →

Related Devices (Code: ITQ)

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.

K831044LIMITED MOTION FUNCTIONAL KNEE BRACEOrthopedic Systems, Inc.K831310BRACE C.T.Innovation Sports, Inc.K823658DELUXE KNEE IMMOBILIZER(UNIVERSAL)Warm & Form, Orthopedic MaterialsK823397ANATOMIC FRACTURE BRACEOrthopedic Systems, Inc.K823159DELUXE KNEE IMMOBILIZERWarm & Form, Orthopedic MaterialsK812423NEOPRENE KNEE SUPPORTSurgical Appliance Industries, Inc.

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.

↑