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FDA 510(k)

TONSIL KNIFE-VARIOUS

K-Number: K841005 · 1984-05-30

ApplicantPremier Dental Products Co.
Decision Date1984-05-30
Product CodeKBQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TONSIL KNIFE-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 1984-05-30 under 510(k) number K841005. The device is classified under product code KBQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TONSIL KNIFE-VARIOUS?

TONSIL KNIFE-VARIOUS is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Premier Dental Products Co.. The 510(k) number is K841005.

When did TONSIL KNIFE-VARIOUS receive FDA 510(k) clearance?

TONSIL KNIFE-VARIOUS received FDA 510(k) clearance on 1984-05-30, under 510(k) number K841005.

Who is the listed applicant for TONSIL KNIFE-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 TONSIL KNIFE-VARIOUS?

The FDA product code for TONSIL KNIFE-VARIOUS is KBQ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 40 devices →

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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