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FDA 510(k)

MICADENT

K-Number: K964059 · 1996-12-19

ApplicantHampton Research
Decision Date1996-12-19
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICADENT is the device name listed in this FDA 510(k) record. The listed applicant is Hampton Research. It received FDA 510(k) clearance on 1996-12-19 under 510(k) number K964059. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICADENT?

MICADENT is a medical device that received FDA 510(k) clearance on 1996-12-19. The listed applicant is Hampton Research. The 510(k) number is K964059.

When did MICADENT receive FDA 510(k) clearance?

MICADENT received FDA 510(k) clearance on 1996-12-19, under 510(k) number K964059.

Who is the listed applicant for MICADENT?

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

What is the FDA product code for MICADENT?

The FDA product code for MICADENT is KOJ.

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Related Devices (Code: KOJ)

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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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