MATCH PRESS PRESSABLE CERAMIC
K-Number: K024250 · 2003-08-25
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Device Summary
Frequently Asked Questions
What is the MATCH PRESS PRESSABLE CERAMIC?
MATCH PRESS PRESSABLE CERAMIC is a medical device that received FDA 510(k) clearance on 2003-08-25. The listed applicant is Davis Schottlander & Davis, Ltd.. The 510(k) number is K024250.
When did MATCH PRESS PRESSABLE CERAMIC receive FDA 510(k) clearance?
MATCH PRESS PRESSABLE CERAMIC received FDA 510(k) clearance on 2003-08-25, under 510(k) number K024250.
Who is the listed applicant for MATCH PRESS PRESSABLE CERAMIC?
The FDA 510(k) record lists Davis Schottlander & Davis, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MATCH PRESS PRESSABLE CERAMIC?
The FDA product code for MATCH PRESS PRESSABLE CERAMIC is EIH.
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 Davis Schottlander & Davis, Ltd. 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: EIH)
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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