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FDA 510(k)

HEMASEAL & CIDE

K-Number: K990779 · 1999-11-17

ApplicantAdvantage Dental Products, Inc.
Decision Date1999-11-17
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HEMASEAL & CIDE is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Dental Products, Inc.. It received FDA 510(k) clearance on 1999-11-17 under 510(k) number K990779. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMASEAL & CIDE?

HEMASEAL & CIDE is a medical device that received FDA 510(k) clearance on 1999-11-17. The listed applicant is Advantage Dental Products, Inc.. The 510(k) number is K990779.

When did HEMASEAL & CIDE receive FDA 510(k) clearance?

HEMASEAL & CIDE received FDA 510(k) clearance on 1999-11-17, under 510(k) number K990779.

Who is the listed applicant for HEMASEAL & CIDE?

The FDA 510(k) record lists Advantage Dental Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMASEAL & CIDE?

The FDA product code for HEMASEAL & CIDE is LBH.

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Other records listing Advantage Dental Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K900389TEMPORARY CROWN MATRIX BUTTONSK890712ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS

Related Devices (Code: LBH)

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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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