RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4
K-Number: K891464 · 1989-05-18
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Device Summary
Frequently Asked Questions
What is the RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4?
RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4 is a medical device that received FDA 510(k) clearance on 1989-05-18. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K891464.
When did RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4 receive FDA 510(k) clearance?
RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4 received FDA 510(k) clearance on 1989-05-18, under 510(k) number K891464.
Who is the listed applicant for RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4?
The FDA 510(k) record lists Confi-Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4?
The FDA product code for RESILIENCE C2, RESILIENCE L3 & RESILIENCE P4 is DYH.
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 Confi-Dental Products Co. 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: DYH)
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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