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FDA 510(k)

DENTAL COMPOSITE RESTORATIVE MATERIAL

K-Number: K790594 · 1979-06-15

ApplicantWallace A. Erickson & Co.
Decision Date1979-06-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL COMPOSITE RESTORATIVE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Wallace A. Erickson & Co.. It received FDA 510(k) clearance on 1979-06-15 under 510(k) number K790594. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL COMPOSITE RESTORATIVE MATERIAL?

DENTAL COMPOSITE RESTORATIVE MATERIAL is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Wallace A. Erickson & Co.. The 510(k) number is K790594.

When did DENTAL COMPOSITE RESTORATIVE MATERIAL receive FDA 510(k) clearance?

DENTAL COMPOSITE RESTORATIVE MATERIAL received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790594.

Who is the listed applicant for DENTAL COMPOSITE RESTORATIVE MATERIAL?

The FDA 510(k) record lists Wallace A. Erickson & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL COMPOSITE RESTORATIVE MATERIAL?

The FDA product code for DENTAL COMPOSITE RESTORATIVE MATERIAL is EBF.

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Other records listing Wallace A. Erickson & Co. 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.

K984503ALPHA BOND DENTIN/ENAMEL BONDING AGENT, MODEL 213-000K963922ALPHA-DENT ROOT CANAL SEALER & FILLERK960667CENTRIX FLOFIL/CENTRIX FLOFIL WITH FLUORIDEK960365ALPHA-DENT HEMA DESENTIZER(748-000)/WITH FLUORIDE(747-000)K960165ALPHA-DENT COMPOSITE SURFACE SEALANTK960122ALPHA-DENT TEMPORARY CROWN AND BRIDGE MATERIAL

View all 32 devices →

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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