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FDA 510(k)

JELDENT MULTICRYL

K-Number: K990056 · 1999-03-25

ApplicantJ.F. Jelenko & Co., Inc.
Decision Date1999-03-25
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JELDENT MULTICRYL is the device name listed in this FDA 510(k) record. The listed applicant is J.F. Jelenko & Co., Inc.. It received FDA 510(k) clearance on 1999-03-25 under 510(k) number K990056. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JELDENT MULTICRYL?

JELDENT MULTICRYL is a medical device that received FDA 510(k) clearance on 1999-03-25. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K990056.

When did JELDENT MULTICRYL receive FDA 510(k) clearance?

JELDENT MULTICRYL received FDA 510(k) clearance on 1999-03-25, under 510(k) number K990056.

Who is the listed applicant for JELDENT MULTICRYL?

The FDA 510(k) record lists J.F. Jelenko & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JELDENT MULTICRYL?

The FDA product code for JELDENT MULTICRYL is EBI.

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Other records listing J.F. Jelenko & Co., Inc. as applicant

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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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