TUTTNAUER LSI (AUTOMATIC)
K-Number: K920478 · 1993-07-08
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Device Summary
Frequently Asked Questions
What is the TUTTNAUER LSI (AUTOMATIC)?
TUTTNAUER LSI (AUTOMATIC) is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Tuttnauer Co. , Ltd.. The 510(k) number is K920478.
When did TUTTNAUER LSI (AUTOMATIC) receive FDA 510(k) clearance?
TUTTNAUER LSI (AUTOMATIC) received FDA 510(k) clearance on 1993-07-08, under 510(k) number K920478.
Who is the listed applicant for TUTTNAUER LSI (AUTOMATIC)?
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 LSI (AUTOMATIC)?
The FDA product code for TUTTNAUER LSI (AUTOMATIC) 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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