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FDA 510(k)

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT

K-Number: K844976 · 1985-04-01

Decision Date1985-04-01
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT 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 1985-04-01 under 510(k) number K844976. The device is classified under product code FSA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT?

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Medi-Man Rehabilitation Products, Inc.. The 510(k) number is K844976.

When did MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT receive FDA 510(k) clearance?

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT received FDA 510(k) clearance on 1985-04-01, under 510(k) number K844976.

Who is the listed applicant for MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT?

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 MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT?

The FDA product code for MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT is FSA.

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.

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.

Related Devices (Code: FSA)

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.

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.

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