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FDA 510(k)

DMV(R) VENEER SUCTION GRIPPER

K-Number: K896565 · 1990-02-02

ApplicantDmv Corp.
Decision Date1990-02-02
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DMV(R) VENEER SUCTION GRIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Dmv Corp.. It received FDA 510(k) clearance on 1990-02-02 under 510(k) number K896565. 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 DMV(R) VENEER SUCTION GRIPPER?

DMV(R) VENEER SUCTION GRIPPER is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Dmv Corp.. The 510(k) number is K896565.

When did DMV(R) VENEER SUCTION GRIPPER receive FDA 510(k) clearance?

DMV(R) VENEER SUCTION GRIPPER received FDA 510(k) clearance on 1990-02-02, under 510(k) number K896565.

Who is the listed applicant for DMV(R) VENEER SUCTION GRIPPER?

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

What is the FDA product code for DMV(R) VENEER SUCTION GRIPPER?

The FDA product code for DMV(R) VENEER SUCTION GRIPPER 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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