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)

A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM

K-Number: K992779 · 2000-01-13

ApplicantMedi-Man Rehabilitation Products, Inc.
Decision Date2000-01-13
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Man Rehabilitation Products, Inc.. It received FDA 510(k) clearance on 2000-01-13 under 510(k) number K992779. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM?

A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM is a medical device that received FDA 510(k) clearance on 2000-01-13. The listed applicant is Medi-Man Rehabilitation Products, Inc.. The 510(k) number is K992779.

When did A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM receive FDA 510(k) clearance?

A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM received FDA 510(k) clearance on 2000-01-13, under 510(k) number K992779.

Who is the listed applicant for A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM?

The FDA 510(k) record lists Medi-Man Rehabilitation Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM?

The FDA product code for A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM is ILJ.

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 Medi-Man Rehabilitation Products, 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.

K925195MALIBU BATHING SYSTEMK924905MEDI-PLINTHK844976MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT

Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, 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.

↑