KIS MT4
K-Number: K960111 · 1996-03-27
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Device Summary
Frequently Asked Questions
What is the KIS MT4?
KIS MT4 is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is The Implant Center of the Palm Beaches. The 510(k) number is K960111.
When did KIS MT4 receive FDA 510(k) clearance?
KIS MT4 received FDA 510(k) clearance on 1996-03-27, under 510(k) number K960111.
Who is the listed applicant for KIS MT4?
The FDA 510(k) record lists The Implant Center of the Palm Beaches as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIS MT4?
The FDA product code for KIS MT4 is DZE.
Other records listing The Implant Center of the Palm Beaches 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: DZE)
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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