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FDA 510(k)

IMPERVA-A

K-Number: K871899 · 1987-07-21

ApplicantShofu Dental Corp.
Decision Date1987-07-21
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPERVA-A is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K871899. 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 IMPERVA-A?

IMPERVA-A is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Shofu Dental Corp.. The 510(k) number is K871899.

When did IMPERVA-A receive FDA 510(k) clearance?

IMPERVA-A received FDA 510(k) clearance on 1987-07-21, under 510(k) number K871899.

Who is the listed applicant for IMPERVA-A?

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

What is the FDA product code for IMPERVA-A?

The FDA product code for IMPERVA-A is EBF.

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Other records listing Shofu Dental 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.

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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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