TITERTEK MICROPLATE WASHER 120
K-Number: K844500 · 1985-01-22
Advertisement
Device Summary
Frequently Asked Questions
What is the TITERTEK MICROPLATE WASHER 120?
TITERTEK MICROPLATE WASHER 120 is a medical device that received FDA 510(k) clearance on 1985-01-22. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K844500.
When did TITERTEK MICROPLATE WASHER 120 receive FDA 510(k) clearance?
TITERTEK MICROPLATE WASHER 120 received FDA 510(k) clearance on 1985-01-22, under 510(k) number K844500.
Who is the listed applicant for TITERTEK MICROPLATE WASHER 120?
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 120?
The FDA product code for TITERTEK MICROPLATE WASHER 120 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.
Advertisement