KAVOKLAVE STEAM AUTOCLAVE
K-Number: K910789 · 1991-08-26
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Device Summary
Frequently Asked Questions
What is the KAVOKLAVE STEAM AUTOCLAVE?
KAVOKLAVE STEAM AUTOCLAVE is a medical device that received FDA 510(k) clearance on 1991-08-26. The listed applicant is Kavo America. The 510(k) number is K910789.
When did KAVOKLAVE STEAM AUTOCLAVE receive FDA 510(k) clearance?
KAVOKLAVE STEAM AUTOCLAVE received FDA 510(k) clearance on 1991-08-26, under 510(k) number K910789.
Who is the listed applicant for KAVOKLAVE STEAM AUTOCLAVE?
The FDA 510(k) record lists Kavo America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAVOKLAVE STEAM AUTOCLAVE?
The FDA product code for KAVOKLAVE STEAM AUTOCLAVE is FLE.
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 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: FLE)
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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