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)

MODEL LTV 1100 VENTILATOR

K-Number: K101643 · 2011-01-26

ApplicantCare Fusion
Decision Date2011-01-26
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL LTV 1100 VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2011-01-26 under 510(k) number K101643. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL LTV 1100 VENTILATOR?

MODEL LTV 1100 VENTILATOR is a medical device that received FDA 510(k) clearance on 2011-01-26. The listed applicant is Care Fusion. The 510(k) number is K101643.

When did MODEL LTV 1100 VENTILATOR receive FDA 510(k) clearance?

MODEL LTV 1100 VENTILATOR received FDA 510(k) clearance on 2011-01-26, under 510(k) number K101643.

Who is the listed applicant for MODEL LTV 1100 VENTILATOR?

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

What is the FDA product code for MODEL LTV 1100 VENTILATOR?

The FDA product code for MODEL LTV 1100 VENTILATOR is CBK.

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 Care Fusion 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 27 devices →

Related Devices (Code: CBK)

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.

↑