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)

VISION PROPHY PASTE WITH FLUORIDE

K-Number: K935925 · 1994-01-26

Decision Date1994-01-26
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VISION PROPHY PASTE WITH FLUORIDE is the device name listed in this FDA 510(k) record. The listed applicant is Block Drug Company, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K935925. 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 VISION PROPHY PASTE WITH FLUORIDE?

VISION PROPHY PASTE WITH FLUORIDE is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Block Drug Company, Inc.. The 510(k) number is K935925.

When did VISION PROPHY PASTE WITH FLUORIDE receive FDA 510(k) clearance?

VISION PROPHY PASTE WITH FLUORIDE received FDA 510(k) clearance on 1994-01-26, under 510(k) number K935925.

Who is the listed applicant for VISION PROPHY PASTE WITH FLUORIDE?

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

What is the FDA product code for VISION PROPHY PASTE WITH FLUORIDE?

The FDA product code for VISION PROPHY PASTE WITH FLUORIDE 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 Block Drug Company, Inc. 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.

View all 10 devices →

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.

↑