FDA 510(k)

DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT

K-Number: K850891 · 1985-03-25

Decision Date1985-03-25

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT 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 1985-03-25 under 510(k) number K850891. 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 MEDIUM D7777, W/L-GLUT?

DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Sigma Chemical Co.. The 510(k) number is K850891.

When did DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT receive FDA 510(k) clearance?

DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850891.

Who is the listed applicant for DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT?

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 MEDIUM D7777, W/L-GLUT?

The FDA product code for DULBECCO'S MODIFIED EAGLE'S MEDIUM D7777, W/L-GLUT is KIT.

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Other records listing Sigma Chemical Co. as applicant

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Related Devices (Code: KIT)

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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.