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FDA 510(k)

KWIKAP

K-Number: K772315 · 1978-01-03

ApplicantDen-Mat Corp.
Decision Date1978-01-03
Product CodeEMB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KWIKAP is the device name listed in this FDA 510(k) record. The listed applicant is Den-Mat Corp.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772315. The device is classified under product code EMB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KWIKAP?

KWIKAP is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Den-Mat Corp.. The 510(k) number is K772315.

When did KWIKAP receive FDA 510(k) clearance?

KWIKAP received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772315.

Who is the listed applicant for KWIKAP?

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

What is the FDA product code for KWIKAP?

The FDA product code for KWIKAP is EMB.

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Other records listing Den-Mat Corp. 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.

K9831061ST IMPRESSIONK895731DEN-MAT CERINATE PORCELAINK895269DEN-MAT LAMI-QUICKK881918LIGHT-CURED ZIONOMER CEMENTK875351DEN-MAT PORETCH (PORCELAIN ETCHANT)K872510DEN-MAT TENURE

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Related Devices (Code: EMB)

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.

K161630Provicol QM PlusVoco GmbHK120695DENTIST IN A BOX DENTAL EMERGENCY KIT PLUS TOOTH TRAUMA CARE KITDentist IN A Box Pty., Ltd.K110759TEMPOCEMDmg USA, Inc.K073539PROVISA CEMCavex Holland BVK020158NON-EUGENOL TEMPORARY CEMENTJ. Morita USA, Inc.K941066DENTAL 911L.A.F. Industries, Inc.

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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