SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM
K-Number: K893811 · 1989-09-07
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Device Summary
Frequently Asked Questions
What is the SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM?
SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM is a medical device that received FDA 510(k) clearance on 1989-09-07. The listed applicant is Sakura Finetek U.S.A., Inc.. The 510(k) number is K893811.
When did SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM receive FDA 510(k) clearance?
SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM received FDA 510(k) clearance on 1989-09-07, under 510(k) number K893811.
Who is the listed applicant for SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM?
The FDA 510(k) record lists Sakura Finetek U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM?
The FDA product code for SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM is JQW.
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 Sakura Finetek U.S.A., Inc. 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: JQW)
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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