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FDA 510(k)

NSI ELT-D DILUTING FLUID 4000ML

K-Number: K844782 · 1985-03-05

Decision Date1985-03-05
Product CodeGIF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

NSI ELT-D DILUTING FLUID 4000ML is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Scientific Industries, Inc.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K844782. The device is classified under product code GIF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NSI ELT-D DILUTING FLUID 4000ML?

NSI ELT-D DILUTING FLUID 4000ML is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Nobel Scientific Industries, Inc.. The 510(k) number is K844782.

When did NSI ELT-D DILUTING FLUID 4000ML receive FDA 510(k) clearance?

NSI ELT-D DILUTING FLUID 4000ML received FDA 510(k) clearance on 1985-03-05, under 510(k) number K844782.

Who is the listed applicant for NSI ELT-D DILUTING FLUID 4000ML?

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

What is the FDA product code for NSI ELT-D DILUTING FLUID 4000ML?

The FDA product code for NSI ELT-D DILUTING FLUID 4000ML is GIF.

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 Nobel Scientific Industries, 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 23 devices →

Related Devices (Code: GIF)

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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