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FDA 510(k)

CIMPAT N

K-Number: K972485 · 1997-09-08

ApplicantArent, Fox, Kintner, Plotkin & Kahn
Decision Date1997-09-08
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CIMPAT N is the device name listed in this FDA 510(k) record. The listed applicant is Arent, Fox, Kintner, Plotkin & Kahn. It received FDA 510(k) clearance on 1997-09-08 under 510(k) number K972485. 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 CIMPAT N?

CIMPAT N is a medical device that received FDA 510(k) clearance on 1997-09-08. The listed applicant is Arent, Fox, Kintner, Plotkin & Kahn. The 510(k) number is K972485.

When did CIMPAT N receive FDA 510(k) clearance?

CIMPAT N received FDA 510(k) clearance on 1997-09-08, under 510(k) number K972485.

Who is the listed applicant for CIMPAT N?

The FDA 510(k) record lists Arent, Fox, Kintner, Plotkin & Kahn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIMPAT N?

The FDA product code for CIMPAT N is EMA.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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