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FDA 510(k)

VASCULON 2 INTRAVENOUS CANNULA

K-Number: K883415 · 1988-10-04

ApplicantOhmeda Medical
Decision Date1988-10-04
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VASCULON 2 INTRAVENOUS CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1988-10-04 under 510(k) number K883415. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULON 2 INTRAVENOUS CANNULA?

VASCULON 2 INTRAVENOUS CANNULA is a medical device that received FDA 510(k) clearance on 1988-10-04. The listed applicant is Ohmeda Medical. The 510(k) number is K883415.

When did VASCULON 2 INTRAVENOUS CANNULA receive FDA 510(k) clearance?

VASCULON 2 INTRAVENOUS CANNULA received FDA 510(k) clearance on 1988-10-04, under 510(k) number K883415.

Who is the listed applicant for VASCULON 2 INTRAVENOUS CANNULA?

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

What is the FDA product code for VASCULON 2 INTRAVENOUS CANNULA?

The FDA product code for VASCULON 2 INTRAVENOUS CANNULA is FOZ.

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Other records listing Ohmeda Medical 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.

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