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FDA 510(k)

KERR GELLED PHOSPHORIC ACID ETCHANT

K-Number: K843026 · 1984-09-27

ApplicantKerr Corporation (Danbury)
Decision Date1984-09-27
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR GELLED PHOSPHORIC ACID ETCHANT is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation (Danbury). It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843026. 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 KERR GELLED PHOSPHORIC ACID ETCHANT?

KERR GELLED PHOSPHORIC ACID ETCHANT is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K843026.

When did KERR GELLED PHOSPHORIC ACID ETCHANT receive FDA 510(k) clearance?

KERR GELLED PHOSPHORIC ACID ETCHANT received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843026.

Who is the listed applicant for KERR GELLED PHOSPHORIC ACID ETCHANT?

The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KERR GELLED PHOSPHORIC ACID ETCHANT?

The FDA product code for KERR GELLED PHOSPHORIC ACID ETCHANT is EBF.

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Other records listing Kerr Corporation (Danbury) 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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