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FDA 510(k)

I NETILMICIN RIA KIT

K-Number: K790514 · 1979-05-03

ApplicantDiagnostic Products Corp.
Decision Date1979-05-03
Product CodeJTB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

I NETILMICIN RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1979-05-03 under 510(k) number K790514. The device is classified under product code JTB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I NETILMICIN RIA KIT?

I NETILMICIN RIA KIT is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K790514.

When did I NETILMICIN RIA KIT receive FDA 510(k) clearance?

I NETILMICIN RIA KIT received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790514.

Who is the listed applicant for I NETILMICIN RIA KIT?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I NETILMICIN RIA KIT?

The FDA product code for I NETILMICIN RIA KIT is JTB.

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Other records listing Diagnostic Products Corp. 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.

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Related Devices (Code: JTB)

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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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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