DENSPRO MEDIUM MINT PROPHY PASTE
K-Number: K923675 · 1992-11-05
Advertisement
Device Summary
Frequently Asked Questions
What is the DENSPRO MEDIUM MINT PROPHY PASTE?
DENSPRO MEDIUM 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 K923675.
When did DENSPRO MEDIUM MINT PROPHY PASTE receive FDA 510(k) clearance?
DENSPRO MEDIUM MINT PROPHY PASTE received FDA 510(k) clearance on 1992-11-05, under 510(k) number K923675.
Who is the listed applicant for DENSPRO MEDIUM 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 MEDIUM MINT PROPHY PASTE?
The FDA product code for DENSPRO MEDIUM 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.
Advertisement