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FDA 510(k)

STACKING MICROPLATE WASHER

K-Number: K915284 · 1992-01-22

Decision Date1992-01-22
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STACKING MICROPLATE WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Denley Instruments, Inc.. It received FDA 510(k) clearance on 1992-01-22 under 510(k) number K915284. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STACKING MICROPLATE WASHER?

STACKING MICROPLATE WASHER is a medical device that received FDA 510(k) clearance on 1992-01-22. The listed applicant is Denley Instruments, Inc.. The 510(k) number is K915284.

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

STACKING MICROPLATE WASHER received FDA 510(k) clearance on 1992-01-22, under 510(k) number K915284.

Who is the listed applicant for STACKING MICROPLATE WASHER?

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

What is the FDA product code for STACKING MICROPLATE WASHER?

The FDA product code for STACKING MICROPLATE WASHER is JQW.

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 Denley Instruments, 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: JQW)

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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