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FDA 510(k)

THE BIONIC EXERCISER

K-Number: K790746 · 1979-05-14

ApplicantScudder Molner Instruments
Decision Date1979-05-14
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE BIONIC EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Scudder Molner Instruments. It received FDA 510(k) clearance on 1979-05-14 under 510(k) number K790746. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BIONIC EXERCISER?

THE BIONIC EXERCISER is a medical device that received FDA 510(k) clearance on 1979-05-14. The listed applicant is Scudder Molner Instruments. The 510(k) number is K790746.

When did THE BIONIC EXERCISER receive FDA 510(k) clearance?

THE BIONIC EXERCISER received FDA 510(k) clearance on 1979-05-14, under 510(k) number K790746.

Who is the listed applicant for THE BIONIC EXERCISER?

The FDA 510(k) record lists Scudder Molner Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE BIONIC EXERCISER?

The FDA product code for THE BIONIC EXERCISER is HCC.

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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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