RSP MEGA SAMPLE PROCESSOR
K-Number: K915492 · 1992-02-21
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Device Summary
Frequently Asked Questions
What is the RSP MEGA SAMPLE PROCESSOR?
RSP MEGA SAMPLE PROCESSOR is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Tecan U.S., Ltd.. The 510(k) number is K915492.
When did RSP MEGA SAMPLE PROCESSOR receive FDA 510(k) clearance?
RSP MEGA SAMPLE PROCESSOR received FDA 510(k) clearance on 1992-02-21, under 510(k) number K915492.
Who is the listed applicant for RSP MEGA SAMPLE PROCESSOR?
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 RSP MEGA SAMPLE PROCESSOR?
The FDA product code for RSP MEGA SAMPLE PROCESSOR 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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