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)

DENSPRO COARSE MINT PROPHY PASTE

K-Number: K923674 · 1992-11-05

ApplicantTeledyne Getz
Decision Date1992-11-05
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENSPRO COARSE MINT PROPHY PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Getz. It received FDA 510(k) clearance on 1992-11-05 under 510(k) number K923674. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENSPRO COARSE MINT PROPHY PASTE?

DENSPRO COARSE MINT PROPHY PASTE is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Teledyne Getz. The 510(k) number is K923674.

When did DENSPRO COARSE MINT PROPHY PASTE receive FDA 510(k) clearance?

DENSPRO COARSE MINT PROPHY PASTE received FDA 510(k) clearance on 1992-11-05, under 510(k) number K923674.

Who is the listed applicant for DENSPRO COARSE MINT PROPHY PASTE?

The FDA 510(k) record lists Teledyne Getz as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENSPRO COARSE MINT PROPHY PASTE?

The FDA product code for DENSPRO COARSE MINT PROPHY PASTE is EJR.

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.

Other records listing Teledyne Getz 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.

Related Devices (Code: EJR)

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.

↑