MATRX DENTAL UNIT
K-Number: K893219 · 1989-08-07
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Device Summary
Frequently Asked Questions
What is the MATRX DENTAL UNIT?
MATRX DENTAL UNIT is a medical device that received FDA 510(k) clearance on 1989-08-07. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K893219.
When did MATRX DENTAL UNIT receive FDA 510(k) clearance?
MATRX DENTAL UNIT received FDA 510(k) clearance on 1989-08-07, under 510(k) number K893219.
Who is the listed applicant for MATRX DENTAL UNIT?
The FDA 510(k) record lists Matrix Medica, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MATRX DENTAL UNIT?
The FDA product code for MATRX DENTAL UNIT 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 Matrix Medica, 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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