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FDA 510(k)

SLT 220 WASHER FOR MICROITITERPLATES

K-Number: K844892 · 1985-02-25

Decision Date1985-02-25
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SLT 220 WASHER FOR MICROITITERPLATES is the device name listed in this FDA 510(k) record. The listed applicant is Slt Labinstruments, Inc.. It received FDA 510(k) clearance on 1985-02-25 under 510(k) number K844892. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT 220 WASHER FOR MICROITITERPLATES?

SLT 220 WASHER FOR MICROITITERPLATES is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Slt Labinstruments, Inc.. The 510(k) number is K844892.

When did SLT 220 WASHER FOR MICROITITERPLATES receive FDA 510(k) clearance?

SLT 220 WASHER FOR MICROITITERPLATES received FDA 510(k) clearance on 1985-02-25, under 510(k) number K844892.

Who is the listed applicant for SLT 220 WASHER FOR MICROITITERPLATES?

The FDA 510(k) record lists Slt Labinstruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLT 220 WASHER FOR MICROITITERPLATES?

The FDA product code for SLT 220 WASHER FOR MICROITITERPLATES is JTZ.

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 Slt Labinstruments, 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 9 devices →

Related Devices (Code: JTZ)

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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