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FDA 510(k)

BISFIL-I LIGHT CURABLE POSTERIOR COMPO

K-Number: K842087 · 1984-07-12

ApplicantBisco, Inc.
Decision Date1984-07-12
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BISFIL-I LIGHT CURABLE POSTERIOR COMPO is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1984-07-12 under 510(k) number K842087. 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 BISFIL-I LIGHT CURABLE POSTERIOR COMPO?

BISFIL-I LIGHT CURABLE POSTERIOR COMPO is a medical device that received FDA 510(k) clearance on 1984-07-12. The listed applicant is Bisco, Inc.. The 510(k) number is K842087.

When did BISFIL-I LIGHT CURABLE POSTERIOR COMPO receive FDA 510(k) clearance?

BISFIL-I LIGHT CURABLE POSTERIOR COMPO received FDA 510(k) clearance on 1984-07-12, under 510(k) number K842087.

Who is the listed applicant for BISFIL-I LIGHT CURABLE POSTERIOR COMPO?

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

What is the FDA product code for BISFIL-I LIGHT CURABLE POSTERIOR COMPO?

The FDA product code for BISFIL-I LIGHT CURABLE POSTERIOR COMPO is EBF.

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Other records listing Bisco, Inc. as applicant

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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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