TITERTEK MICROPLATE WASHER S-12
K-Number: K862066 · 1986-06-05
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Device Summary
Frequently Asked Questions
What is the TITERTEK MICROPLATE WASHER S-12?
TITERTEK MICROPLATE WASHER S-12 is a medical device that received FDA 510(k) clearance on 1986-06-05. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K862066.
When did TITERTEK MICROPLATE WASHER S-12 receive FDA 510(k) clearance?
TITERTEK MICROPLATE WASHER S-12 received FDA 510(k) clearance on 1986-06-05, under 510(k) number K862066.
Who is the listed applicant for TITERTEK MICROPLATE WASHER S-12?
The FDA 510(k) record lists Flow Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITERTEK MICROPLATE WASHER S-12?
The FDA product code for TITERTEK MICROPLATE WASHER S-12 is JTC.
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 Flow Laboratories, 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: JTC)
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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