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FDA 510(k)

MEDICON VIPAIR HIGH SPEED SYSTEM

K-Number: K042974 · 2005-01-13

ApplicantMedicon EG
Decision Date2005-01-13
Product CodeHBB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDICON VIPAIR HIGH SPEED SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medicon EG. It received FDA 510(k) clearance on 2005-01-13 under 510(k) number K042974. The device is classified under product code HBB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICON VIPAIR HIGH SPEED SYSTEM?

MEDICON VIPAIR HIGH SPEED SYSTEM is a medical device that received FDA 510(k) clearance on 2005-01-13. The listed applicant is Medicon EG. The 510(k) number is K042974.

When did MEDICON VIPAIR HIGH SPEED SYSTEM receive FDA 510(k) clearance?

MEDICON VIPAIR HIGH SPEED SYSTEM received FDA 510(k) clearance on 2005-01-13, under 510(k) number K042974.

Who is the listed applicant for MEDICON VIPAIR HIGH SPEED SYSTEM?

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

What is the FDA product code for MEDICON VIPAIR HIGH SPEED SYSTEM?

The FDA product code for MEDICON VIPAIR HIGH SPEED SYSTEM is HBB.

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Other records listing Medicon EG as applicant

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Related Devices (Code: HBB)

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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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