FDA 510(k)

VENOSET MULTI-MED PIGGYBACK W/IVEX-2

K-Number: K833740 · 1983-12-27

Decision Date1983-12-27

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VENOSET MULTI-MED PIGGYBACK W/IVEX-2 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833740. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOSET MULTI-MED PIGGYBACK W/IVEX-2?

VENOSET MULTI-MED PIGGYBACK W/IVEX-2 is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Abbott Laboratories. The 510(k) number is K833740.

When did VENOSET MULTI-MED PIGGYBACK W/IVEX-2 receive FDA 510(k) clearance?

VENOSET MULTI-MED PIGGYBACK W/IVEX-2 received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833740.

Who is the listed applicant for VENOSET MULTI-MED PIGGYBACK W/IVEX-2?

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

What is the FDA product code for VENOSET MULTI-MED PIGGYBACK W/IVEX-2?

The FDA product code for VENOSET MULTI-MED PIGGYBACK W/IVEX-2 is FPA.

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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.