FDA 510(k)

INTRACATH-DA INTRAVENOUS CATH. PLACEMENT

K-Number: K823064 · 1983-01-27

Decision Date1983-01-27

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

INTRACATH-DA INTRAVENOUS CATH. PLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1983-01-27 under 510(k) number K823064. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRACATH-DA INTRAVENOUS CATH. PLACEMENT?

INTRACATH-DA INTRAVENOUS CATH. PLACEMENT is a medical device that received FDA 510(k) clearance on 1983-01-27. The listed applicant is Parke-Davis Co.. The 510(k) number is K823064.

When did INTRACATH-DA INTRAVENOUS CATH. PLACEMENT receive FDA 510(k) clearance?

INTRACATH-DA INTRAVENOUS CATH. PLACEMENT received FDA 510(k) clearance on 1983-01-27, under 510(k) number K823064.

Who is the listed applicant for INTRACATH-DA INTRAVENOUS CATH. PLACEMENT?

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

What is the FDA product code for INTRACATH-DA INTRAVENOUS CATH. PLACEMENT?

The FDA product code for INTRACATH-DA INTRAVENOUS CATH. PLACEMENT is DQO.

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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.