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FDA 510(k)

BIOCELLECT -PERIO

K-Number: K020396 · 2002-04-10

ApplicantImtec Corp.
Decision Date2002-04-10
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIOCELLECT -PERIO is the device name listed in this FDA 510(k) record. The listed applicant is Imtec Corp.. It received FDA 510(k) clearance on 2002-04-10 under 510(k) number K020396. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOCELLECT -PERIO?

BIOCELLECT -PERIO is a medical device that received FDA 510(k) clearance on 2002-04-10. The listed applicant is Imtec Corp.. The 510(k) number is K020396.

When did BIOCELLECT -PERIO receive FDA 510(k) clearance?

BIOCELLECT -PERIO received FDA 510(k) clearance on 2002-04-10, under 510(k) number K020396.

Who is the listed applicant for BIOCELLECT -PERIO?

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

What is the FDA product code for BIOCELLECT -PERIO?

The FDA product code for BIOCELLECT -PERIO is LYC.

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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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