Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE PROPHY HANDPIECE

K-Number: K954012 · 1995-11-08

Decision Date1995-11-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PROPHY HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Denticator Intl., Inc.. It received FDA 510(k) clearance on 1995-11-08 under 510(k) number K954012. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE PROPHY HANDPIECE?

DISPOSABLE PROPHY HANDPIECE is a medical device that received FDA 510(k) clearance on 1995-11-08. The listed applicant is Denticator Intl., Inc.. The 510(k) number is K954012.

When did DISPOSABLE PROPHY HANDPIECE receive FDA 510(k) clearance?

DISPOSABLE PROPHY HANDPIECE received FDA 510(k) clearance on 1995-11-08, under 510(k) number K954012.

Who is the listed applicant for DISPOSABLE PROPHY HANDPIECE?

The FDA 510(k) record lists Denticator Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE PROPHY HANDPIECE?

The FDA product code for DISPOSABLE PROPHY HANDPIECE is EFB.

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.

Related Devices (Code: EFB)

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.

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.

↑