DENTAPURE DP40 CARTRIDGE
K-Number: K992868 · 1999-09-07
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Device Summary
Frequently Asked Questions
What is the DENTAPURE DP40 CARTRIDGE?
DENTAPURE DP40 CARTRIDGE is a medical device that received FDA 510(k) clearance on 1999-09-07. The listed applicant is Mrlb Intl., Inc.. The 510(k) number is K992868.
When did DENTAPURE DP40 CARTRIDGE receive FDA 510(k) clearance?
DENTAPURE DP40 CARTRIDGE received FDA 510(k) clearance on 1999-09-07, under 510(k) number K992868.
Who is the listed applicant for DENTAPURE DP40 CARTRIDGE?
The FDA 510(k) record lists Mrlb Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAPURE DP40 CARTRIDGE?
The FDA product code for DENTAPURE DP40 CARTRIDGE is EIA.
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 Mrlb Intl., 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.
Related Devices (Code: EIA)
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.
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