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FDA 510(k)

THE DIRECTION DIAL

K-Number: K882309 · 1988-06-23

ApplicantLawhorn Innovations
Decision Date1988-06-23
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE DIRECTION DIAL is the device name listed in this FDA 510(k) record. The listed applicant is Lawhorn Innovations. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K882309. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE DIRECTION DIAL?

THE DIRECTION DIAL is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Lawhorn Innovations. The 510(k) number is K882309.

When did THE DIRECTION DIAL receive FDA 510(k) clearance?

THE DIRECTION DIAL received FDA 510(k) clearance on 1988-06-23, under 510(k) number K882309.

Who is the listed applicant for THE DIRECTION DIAL?

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

What is the FDA product code for THE DIRECTION DIAL?

The FDA product code for THE DIRECTION DIAL is EKJ.

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Related Devices (Code: EKJ)

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.

K961714ASEPTYLUM, UNI-CARRIERDistriflor S.A.K953707MEDTROL DENTAL KITMedtrol, Inc.K945815DENTAL KITConstancy Ent., Inc.K951607SUREFLEX FILESDentsply Intl.K945077INSTRUMENT,FILLING,PLASTIC,DENTALWorldwide Dental, Inc.K943820STAT PAKMagnum Instruments, Inc.

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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