Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VENTILAIR II MEDICAL AIR COMPRESSOR

K-Number: K041781 · 2005-03-14

Decision Date2005-03-14
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILAIR II MEDICAL AIR COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Medical AG. It received FDA 510(k) clearance on 2005-03-14 under 510(k) number K041781. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTILAIR II MEDICAL AIR COMPRESSOR?

VENTILAIR II MEDICAL AIR COMPRESSOR is a medical device that received FDA 510(k) clearance on 2005-03-14. The listed applicant is Hamilton Medical AG. The 510(k) number is K041781.

When did VENTILAIR II MEDICAL AIR COMPRESSOR receive FDA 510(k) clearance?

VENTILAIR II MEDICAL AIR COMPRESSOR received FDA 510(k) clearance on 2005-03-14, under 510(k) number K041781.

Who is the listed applicant for VENTILAIR II MEDICAL AIR COMPRESSOR?

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

What is the FDA product code for VENTILAIR II MEDICAL AIR COMPRESSOR?

The FDA product code for VENTILAIR II MEDICAL AIR COMPRESSOR is BTI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Hamilton Medical AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 29 devices →

Related Devices (Code: BTI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑