KAVO ERGOCOM/ERGOCAM
K-Number: K050744 · 2005-04-21
Advertisement
Device Summary
Frequently Asked Questions
What is the KAVO ERGOCOM/ERGOCAM?
KAVO ERGOCOM/ERGOCAM is a medical device that received FDA 510(k) clearance on 2005-04-21. The listed applicant is Kavo America Corporation. The 510(k) number is K050744.
When did KAVO ERGOCOM/ERGOCAM receive FDA 510(k) clearance?
KAVO ERGOCOM/ERGOCAM received FDA 510(k) clearance on 2005-04-21, under 510(k) number K050744.
Who is the listed applicant for KAVO ERGOCOM/ERGOCAM?
The FDA 510(k) record lists Kavo America Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAVO ERGOCOM/ERGOCAM?
The FDA product code for KAVO ERGOCOM/ERGOCAM is LLZ.
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 Kavo America Corporation 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: LLZ)
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.
Advertisement