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FDA 510(k)

HOLD-FAST DENTURE ADHESIVE

K-Number: K884999 · 1989-02-24

ApplicantIodent, Co.
Decision Date1989-02-24
Product CodeKOL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HOLD-FAST DENTURE ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Iodent, Co.. It received FDA 510(k) clearance on 1989-02-24 under 510(k) number K884999. The device is classified under product code KOL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLD-FAST DENTURE ADHESIVE?

HOLD-FAST DENTURE ADHESIVE is a medical device that received FDA 510(k) clearance on 1989-02-24. The listed applicant is Iodent, Co.. The 510(k) number is K884999.

When did HOLD-FAST DENTURE ADHESIVE receive FDA 510(k) clearance?

HOLD-FAST DENTURE ADHESIVE received FDA 510(k) clearance on 1989-02-24, under 510(k) number K884999.

Who is the listed applicant for HOLD-FAST DENTURE ADHESIVE?

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

What is the FDA product code for HOLD-FAST DENTURE ADHESIVE?

The FDA product code for HOLD-FAST DENTURE ADHESIVE is KOL.

Related Clinical Trials

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.

Related Devices (Code: KOL)

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.

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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