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FDA 510(k)

WRIGHTS STAIN SOLUTION

K-Number: K843051 · 1984-08-03

ApplicantReagent Laboratory, Inc.
Decision Date1984-08-03
Product Code
DecisionUnknown

Device Summary

WRIGHTS STAIN SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Reagent Laboratory, Inc.. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K843051. FDA Decision: Unknown.

Frequently Asked Questions

What is the WRIGHTS STAIN SOLUTION?

WRIGHTS STAIN SOLUTION is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Reagent Laboratory, Inc.. The 510(k) number is K843051.

When did WRIGHTS STAIN SOLUTION receive FDA 510(k) clearance?

WRIGHTS STAIN SOLUTION received FDA 510(k) clearance on 1984-08-03, under 510(k) number K843051.

Who is the listed applicant for WRIGHTS STAIN SOLUTION?

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

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Other records listing Reagent Laboratory, 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.

K863502SOLUTION B- NA 50MEQ/L, K 40 MEQ/LK863503HEMOLYSEK863550POTASSIUM HYDROXIDE 10% W/VK860143URINE DILUENT-FOR USE WITH ION SELECTIVE ELECTRODEK842982FORMALIN BUFFEREDK842785STAIN, METHYLENE BLUE-EOSIN

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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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