TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500
K-Number: K854406 · 1986-02-10
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Device Summary
Frequently Asked Questions
What is the TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500?
TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500 is a medical device that received FDA 510(k) clearance on 1986-02-10. The listed applicant is Tecan U.S., Ltd.. The 510(k) number is K854406.
When did TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500 receive FDA 510(k) clearance?
TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500 received FDA 510(k) clearance on 1986-02-10, under 510(k) number K854406.
Who is the listed applicant for TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500?
The FDA 510(k) record lists Tecan U.S., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500?
The FDA product code for TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500 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 Tecan U.S., 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: 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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