TUTTNAUER PRE-VACUUM AUTOCLAVE
K-Number: K850264 · 1985-06-04
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Device Summary
Frequently Asked Questions
What is the TUTTNAUER PRE-VACUUM AUTOCLAVE?
TUTTNAUER PRE-VACUUM AUTOCLAVE is a medical device that received FDA 510(k) clearance on 1985-06-04. The listed applicant is Tuttnauer Co. , Ltd.. The 510(k) number is K850264.
When did TUTTNAUER PRE-VACUUM AUTOCLAVE receive FDA 510(k) clearance?
TUTTNAUER PRE-VACUUM AUTOCLAVE received FDA 510(k) clearance on 1985-06-04, under 510(k) number K850264.
Who is the listed applicant for TUTTNAUER PRE-VACUUM AUTOCLAVE?
The FDA 510(k) record lists Tuttnauer Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUTTNAUER PRE-VACUUM AUTOCLAVE?
The FDA product code for TUTTNAUER PRE-VACUUM 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 Tuttnauer Co. , 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: 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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