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FDA 510(k)

SLT MICROPLATE WASHER

K-Number: K910740 · 1991-03-27

ApplicantTecan U.S., Ltd.
Decision Date1991-03-27
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SLT MICROPLATE WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Tecan U.S., Ltd.. It received FDA 510(k) clearance on 1991-03-27 under 510(k) number K910740. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT MICROPLATE WASHER?

SLT MICROPLATE WASHER is a medical device that received FDA 510(k) clearance on 1991-03-27. The listed applicant is Tecan U.S., Ltd.. The 510(k) number is K910740.

When did SLT MICROPLATE WASHER receive FDA 510(k) clearance?

SLT MICROPLATE WASHER received FDA 510(k) clearance on 1991-03-27, under 510(k) number K910740.

Who is the listed applicant for SLT MICROPLATE WASHER?

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 SLT MICROPLATE WASHER?

The FDA product code for SLT MICROPLATE WASHER is JJQ.

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.

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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.

K933996PROFIBLOTK915492RSP MEGA SAMPLE PROCESSORK912036ROBOTIC SAMPLE PROCESSORK894126ROBOTIC SAMPLE PROCESSORK854406TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500

Related Devices (Code: JJQ)

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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