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FDA 510(k)

STEADFAST DENTURE ADHESIVE POWDER

K-Number: K910216 · 1991-03-29

ApplicantStiefel Research Institute, Inc.
Decision Date1991-03-29
Product CodeKOM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STEADFAST DENTURE ADHESIVE POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Stiefel Research Institute, Inc.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K910216. The device is classified under product code KOM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEADFAST DENTURE ADHESIVE POWDER?

STEADFAST DENTURE ADHESIVE POWDER is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Stiefel Research Institute, Inc.. The 510(k) number is K910216.

When did STEADFAST DENTURE ADHESIVE POWDER receive FDA 510(k) clearance?

STEADFAST DENTURE ADHESIVE POWDER received FDA 510(k) clearance on 1991-03-29, under 510(k) number K910216.

Who is the listed applicant for STEADFAST DENTURE ADHESIVE POWDER?

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

What is the FDA product code for STEADFAST DENTURE ADHESIVE POWDER?

The FDA product code for STEADFAST DENTURE ADHESIVE POWDER is KOM.

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Other records listing Stiefel Research Institute, 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.

K914591L.C.S. 2000 SYSTEMK895818STEADFAST DENTURE ADHESIVE CREAMK895817HERMAL WOUND CARE KITK896724CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.K893996CUSIS ULTRASOUND SKIN IMAGING SYSTEM

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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