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FDA 510(k)

HOYER ONE-TOUCH POWER LIFTER

K-Number: K860837 · 1986-03-27

ApplicantTed Hoyer & Co., Inc.
Decision Date1986-03-27
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HOYER ONE-TOUCH POWER LIFTER is the device name listed in this FDA 510(k) record. The listed applicant is Ted Hoyer & Co., Inc.. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K860837. 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 HOYER ONE-TOUCH POWER LIFTER?

HOYER ONE-TOUCH POWER LIFTER is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Ted Hoyer & Co., Inc.. The 510(k) number is K860837.

When did HOYER ONE-TOUCH POWER LIFTER receive FDA 510(k) clearance?

HOYER ONE-TOUCH POWER LIFTER received FDA 510(k) clearance on 1986-03-27, under 510(k) number K860837.

Who is the listed applicant for HOYER ONE-TOUCH POWER LIFTER?

The FDA 510(k) record lists Ted Hoyer & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOYER ONE-TOUCH POWER LIFTER?

The FDA product code for HOYER ONE-TOUCH POWER LIFTER 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.

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Other records listing Ted Hoyer & Co., 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.

K862477HOYER DIGITAL ELECTRONIC SCALE

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.K851844MOLIFTMadshus A/SK844976MEDI-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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