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FDA 510(k)

DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX

K-Number: K843086 · 1984-08-28

Decision Date1984-08-28
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1984-08-28 under 510(k) number K843086. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX?

DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX is a medical device that received FDA 510(k) clearance on 1984-08-28. The listed applicant is Sigma Chemical Co.. The 510(k) number is K843086.

When did DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX receive FDA 510(k) clearance?

DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX received FDA 510(k) clearance on 1984-08-28, under 510(k) number K843086.

Who is the listed applicant for DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX?

The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX?

The FDA product code for DULBECCO'S MODIFIED EAGLE'S NUTIRENT MIX is KIT.

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 Sigma Chemical Co. 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 231 devices →

Related Devices (Code: KIT)

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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