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FDA 510(k)

CRYSTALLINE C2 AND CRYSTALLINE L3

K-Number: K894890 · 1989-10-27

ApplicantConfi-Dental Products Co.
Decision Date1989-10-27
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CRYSTALLINE C2 AND CRYSTALLINE L3 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 1989-10-27 under 510(k) number K894890. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYSTALLINE C2 AND CRYSTALLINE L3?

CRYSTALLINE C2 AND CRYSTALLINE L3 is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K894890.

When did CRYSTALLINE C2 AND CRYSTALLINE L3 receive FDA 510(k) clearance?

CRYSTALLINE C2 AND CRYSTALLINE L3 received FDA 510(k) clearance on 1989-10-27, under 510(k) number K894890.

Who is the listed applicant for CRYSTALLINE C2 AND CRYSTALLINE L3?

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 C2 AND CRYSTALLINE L3?

The FDA product code for CRYSTALLINE C2 AND CRYSTALLINE L3 is EBF.

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Other records listing Confi-Dental Products Co. as applicant

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Related Devices (Code: EBF)

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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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