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FDA 510(k)

CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE

K-Number: K935714 · 1994-01-21

ApplicantConfi-Dental Products Co.
Decision Date1994-01-21
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE is the device name listed in this FDA 510(k) record. The listed applicant is Confi-Dental Products Co.. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K935714. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE?

CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K935714.

When did CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE receive FDA 510(k) clearance?

CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE received FDA 510(k) clearance on 1994-01-21, under 510(k) number K935714.

Who is the listed applicant for CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE?

The FDA 510(k) record lists Confi-Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE?

The FDA product code for CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE is DYH.

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Other records listing Confi-Dental Products Co. as applicant

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Related Devices (Code: DYH)

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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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