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FDA 510(k)

RAT LIVER NUCLEI TEST SYSTEM

K-Number: K870732 · 1987-03-10

ApplicantVal Tech Diagnostics, Inc.
Decision Date1987-03-10
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RAT LIVER NUCLEI TEST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Val Tech Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-03-10 under 510(k) number K870732. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAT LIVER NUCLEI TEST SYSTEM?

RAT LIVER NUCLEI TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1987-03-10. The listed applicant is Val Tech Diagnostics, Inc.. The 510(k) number is K870732.

When did RAT LIVER NUCLEI TEST SYSTEM receive FDA 510(k) clearance?

RAT LIVER NUCLEI TEST SYSTEM received FDA 510(k) clearance on 1987-03-10, under 510(k) number K870732.

Who is the listed applicant for RAT LIVER NUCLEI TEST SYSTEM?

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

What is the FDA product code for RAT LIVER NUCLEI TEST SYSTEM?

The FDA product code for RAT LIVER NUCLEI TEST SYSTEM is DHN.

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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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