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FDA 510(k)

THE SOFT PEDAL

K-Number: K821696 · 1982-07-14

ApplicantHabco Products, Inc.
Decision Date1982-07-14
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE SOFT PEDAL is the device name listed in this FDA 510(k) record. The listed applicant is Habco Products, Inc.. It received FDA 510(k) clearance on 1982-07-14 under 510(k) number K821696. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SOFT PEDAL?

THE SOFT PEDAL is a medical device that received FDA 510(k) clearance on 1982-07-14. The listed applicant is Habco Products, Inc.. The 510(k) number is K821696.

When did THE SOFT PEDAL receive FDA 510(k) clearance?

THE SOFT PEDAL received FDA 510(k) clearance on 1982-07-14, under 510(k) number K821696.

Who is the listed applicant for THE SOFT PEDAL?

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

What is the FDA product code for THE SOFT PEDAL?

The FDA product code for THE SOFT PEDAL is JOW.

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Related Devices (Code: JOW)

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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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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