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FDA 510(k)

LC DENTAL HAND INSTRUMENT

K-Number: K935217 · 1994-01-05

ApplicantL.C. Dental
Decision Date1994-01-05
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LC DENTAL HAND INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is L.C. Dental. It received FDA 510(k) clearance on 1994-01-05 under 510(k) number K935217. 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 LC DENTAL HAND INSTRUMENT?

LC DENTAL HAND INSTRUMENT is a medical device that received FDA 510(k) clearance on 1994-01-05. The listed applicant is L.C. Dental. The 510(k) number is K935217.

When did LC DENTAL HAND INSTRUMENT receive FDA 510(k) clearance?

LC DENTAL HAND INSTRUMENT received FDA 510(k) clearance on 1994-01-05, under 510(k) number K935217.

Who is the listed applicant for LC DENTAL HAND INSTRUMENT?

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

What is the FDA product code for LC DENTAL HAND INSTRUMENT?

The FDA product code for LC DENTAL HAND INSTRUMENT is EKJ.

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 L.C. Dental 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.

K923384ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED

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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