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FDA 510(k)

XR PRIMER

K-Number: K880684 · 1988-05-11

ApplicantKerr Corporation (Danbury)
Decision Date1988-05-11
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

XR PRIMER 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 1988-05-11 under 510(k) number K880684. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XR PRIMER?

XR PRIMER is a medical device that received FDA 510(k) clearance on 1988-05-11. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K880684.

When did XR PRIMER receive FDA 510(k) clearance?

XR PRIMER received FDA 510(k) clearance on 1988-05-11, under 510(k) number K880684.

Who is the listed applicant for XR PRIMER?

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 XR PRIMER?

The FDA product code for XR PRIMER is KLE.

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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.

K051545L.E. DEMETRON IIK020091OPTILUX 501K951663TYTIN RK951511TYTIN ADMIXK942480M4 CONTRA-ANGLE HANDPIECEK940513OPTIBOND

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Related Devices (Code: KLE)

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.

K262252MPa Max adhesiveDen-Mat Holdings, LLCK260485Any-EtchMediclus Co., Ltd.K260430Porcelain Etch GelBelport Company, Inc., Gingi-PakK252450Adhese 2Ivoclar Vivadent, Inc.K260682Bond-PR™ Universal AdhesivePremier Dental Products CompanyK251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg.

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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