THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR
K-Number: K862506 · 1986-07-29
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Device Summary
Frequently Asked Questions
What is the THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR?
THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR is a medical device that received FDA 510(k) clearance on 1986-07-29. The listed applicant is Millipore Corp.. The 510(k) number is K862506.
When did THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR receive FDA 510(k) clearance?
THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR received FDA 510(k) clearance on 1986-07-29, under 510(k) number K862506.
Who is the listed applicant for THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR?
The FDA 510(k) record lists Millipore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR?
The FDA product code for THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTOR is KIE.
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 Millipore Corp. 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: KIE)
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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