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FDA 510(k)

KERR RESIN BONDED BRIDGE CEMENT

K-Number: K840407 · 1984-05-21

ApplicantSybron Corp.
Decision Date1984-05-21
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR RESIN BONDED BRIDGE CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1984-05-21 under 510(k) number K840407. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERR RESIN BONDED BRIDGE CEMENT?

KERR RESIN BONDED BRIDGE CEMENT is a medical device that received FDA 510(k) clearance on 1984-05-21. The listed applicant is Sybron Corp.. The 510(k) number is K840407.

When did KERR RESIN BONDED BRIDGE CEMENT receive FDA 510(k) clearance?

KERR RESIN BONDED BRIDGE CEMENT received FDA 510(k) clearance on 1984-05-21, under 510(k) number K840407.

Who is the listed applicant for KERR RESIN BONDED BRIDGE CEMENT?

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

What is the FDA product code for KERR RESIN BONDED BRIDGE CEMENT?

The FDA product code for KERR RESIN BONDED BRIDGE CEMENT is EMA.

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Other records listing Sybron 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.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

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Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, 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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