FDA 510(k)

INTRAVENOUS START KIT

K-Number: K843813 · 1984-12-05

Decision Date1984-12-05

Product Code

DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab, Inc.. It received FDA 510(k) clearance on 1984-12-05 under 510(k) number K843813. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAVENOUS START KIT?

INTRAVENOUS START KIT is a medical device that received FDA 510(k) clearance on 1984-12-05. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K843813.

When did INTRAVENOUS START KIT receive FDA 510(k) clearance?

INTRAVENOUS START KIT received FDA 510(k) clearance on 1984-12-05, under 510(k) number K843813.

Who is the listed applicant for INTRAVENOUS START KIT?

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

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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.