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)

WILLIAMS BELT & BOOT

K-Number: K891387 · 1989-05-23

ApplicantArthro-Medic, Inc.
Decision Date1989-05-23
Product CodeJEB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WILLIAMS BELT & BOOT is the device name listed in this FDA 510(k) record. The listed applicant is Arthro-Medic, Inc.. It received FDA 510(k) clearance on 1989-05-23 under 510(k) number K891387. The device is classified under product code JEB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS BELT & BOOT?

WILLIAMS BELT & BOOT is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Arthro-Medic, Inc.. The 510(k) number is K891387.

When did WILLIAMS BELT & BOOT receive FDA 510(k) clearance?

WILLIAMS BELT & BOOT received FDA 510(k) clearance on 1989-05-23, under 510(k) number K891387.

Who is the listed applicant for WILLIAMS BELT & BOOT?

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

What is the FDA product code for WILLIAMS BELT & BOOT?

The FDA product code for WILLIAMS BELT & BOOT is JEB.

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 Arthro-Medic, 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.

K933597AQUA+TFILTERHME/THME/AQUA+TFILTERHCH/THCHK893597HYDRAULIC IV POLEK893598HYDRAULIC FOOT OPERATED STOOL

Related Devices (Code: JEB)

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.

K905816ORTHOVISION TABLEAmerican Sterilizer Co.K900405SCHOLTEN FRAMEScholten Surgical Instruments, Inc.K891917ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.K881101K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.K880263OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, Inc.K873275EXTENSION TABLE 1417Stierlen-Maquet AG

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.

↑