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FDA 510(k)

SILICONE MIRROR

K-Number: K932511 · 1993-11-05

ApplicantMoyco Industries, Inc.
Decision Date1993-11-05
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SILICONE MIRROR is the device name listed in this FDA 510(k) record. The listed applicant is Moyco Industries, Inc.. It received FDA 510(k) clearance on 1993-11-05 under 510(k) number K932511. 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 SILICONE MIRROR?

SILICONE MIRROR is a medical device that received FDA 510(k) clearance on 1993-11-05. The listed applicant is Moyco Industries, Inc.. The 510(k) number is K932511.

When did SILICONE MIRROR receive FDA 510(k) clearance?

SILICONE MIRROR received FDA 510(k) clearance on 1993-11-05, under 510(k) number K932511.

Who is the listed applicant for SILICONE MIRROR?

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

What is the FDA product code for SILICONE MIRROR?

The FDA product code for SILICONE MIRROR is EKJ.

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Other records listing Moyco Industries, Inc. 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.

K833558X-RAY SHIELDK821444COLORED WEDGE USED TO SEPARATE TEETHK821629FIXIDENTK810839SPOTARK810912ALLOY COMPOSITE POLISH

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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