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FDA 510(k)

PROBES, VARIOUS

K-Number: K841003 · 1984-03-20

ApplicantPremier Dental Products Co.
Decision Date1984-03-20
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROBES, VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1984-03-20 under 510(k) number K841003. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROBES, VARIOUS?

PROBES, VARIOUS is a medical device that received FDA 510(k) clearance on 1984-03-20. The listed applicant is Premier Dental Products Co.. The 510(k) number is K841003.

When did PROBES, VARIOUS receive FDA 510(k) clearance?

PROBES, VARIOUS received FDA 510(k) clearance on 1984-03-20, under 510(k) number K841003.

Who is the listed applicant for PROBES, VARIOUS?

The FDA 510(k) record lists Premier Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROBES, VARIOUS?

The FDA product code for PROBES, VARIOUS is KOA.

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Other records listing Premier Dental Products Co. 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.

K132526KNIT-PAK+K131212PREMIER CERAMIC PRIMERK083695TRAXODENTK062683ENAMEL PRO VARNISHK062166ENAMEL PROK061998PREMIER SELF-ETCHING BOND ENHANCER

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Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, 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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