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FDA 510(k)

VERIDENT PLUS, OPTIFORM

K-Number: K940244 · 1994-05-02

ApplicantLactona Corp.
Decision Date1994-05-02
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERIDENT PLUS, OPTIFORM is the device name listed in this FDA 510(k) record. The listed applicant is Lactona Corp.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K940244. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIDENT PLUS, OPTIFORM?

VERIDENT PLUS, OPTIFORM is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Lactona Corp.. The 510(k) number is K940244.

When did VERIDENT PLUS, OPTIFORM receive FDA 510(k) clearance?

VERIDENT PLUS, OPTIFORM received FDA 510(k) clearance on 1994-05-02, under 510(k) number K940244.

Who is the listed applicant for VERIDENT PLUS, OPTIFORM?

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

What is the FDA product code for VERIDENT PLUS, OPTIFORM?

The FDA product code for VERIDENT PLUS, OPTIFORM is ELM.

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Related Devices (Code: ELM)

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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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