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FDA 510(k)

TITERTEK MICROPLATE WASHER S-12

K-Number: K862066 · 1986-06-05

Decision Date1986-06-05
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TITERTEK MICROPLATE WASHER S-12 is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1986-06-05 under 510(k) number K862066. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 57 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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