FDA 510(k)

CELLGRO HEPES BUFFER SOLUTION

K-Number: K860623 · 1986-03-03

Decision Date1986-03-03

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

CELLGRO HEPES BUFFER SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Mediatech, Inc.. It received FDA 510(k) clearance on 1986-03-03 under 510(k) number K860623. 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 CELLGRO HEPES BUFFER SOLUTION?

CELLGRO HEPES BUFFER SOLUTION is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Mediatech, Inc.. The 510(k) number is K860623.

When did CELLGRO HEPES BUFFER SOLUTION receive FDA 510(k) clearance?

CELLGRO HEPES BUFFER SOLUTION received FDA 510(k) clearance on 1986-03-03, under 510(k) number K860623.

Who is the listed applicant for CELLGRO HEPES BUFFER SOLUTION?

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

What is the FDA product code for CELLGRO HEPES BUFFER SOLUTION?

The FDA product code for CELLGRO HEPES BUFFER SOLUTION is KIT.

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Other records listing Mediatech, Inc. 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.