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FDA 510(k)

MOLIFT

K-Number: K851844 · 1985-05-17

ApplicantMadshus A/S
Decision Date1985-05-17
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MOLIFT is the device name listed in this FDA 510(k) record. The listed applicant is Madshus A/S. It received FDA 510(k) clearance on 1985-05-17 under 510(k) number K851844. 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 MOLIFT?

MOLIFT is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Madshus A/S. The 510(k) number is K851844.

When did MOLIFT receive FDA 510(k) clearance?

MOLIFT received FDA 510(k) clearance on 1985-05-17, under 510(k) number K851844.

Who is the listed applicant for MOLIFT?

The FDA 510(k) record lists Madshus A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOLIFT?

The FDA product code for MOLIFT is FSA.

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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.

K942807SURGICAL LIFT SHEETSurgin Surgical Instrumentation, Inc.K930625SANITAS PATIENT LIFTDutton-Lainson Co.K902141ANOLIFT - PORTABLE & ANOLIFT - GANTRYAnodyne Corp.K860837HOYER ONE-TOUCH POWER LIFTERTed Hoyer & Co., Inc.K844976MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFTMedi-Man Rehabilitation Products, Inc.K841395SHOWER TROLLEYSetma, 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.

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