FDA 510(k)

DEXTROSE

K-Number: K833214 · 1983-10-27

Decision Date1983-10-27

Product Code

DecisionSubstantially Equivalent

Device Summary

DEXTROSE is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K833214. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXTROSE?

DEXTROSE is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833214.

When did DEXTROSE receive FDA 510(k) clearance?

DEXTROSE received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833214.

Who is the listed applicant for DEXTROSE?

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

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Other records listing Acumedia Manufacturers, Inc. as applicant

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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.