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)

MAX TRANSPORT VENTILATOR

K-Number: K900465 · 1990-06-18

Decision Date1990-06-18
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MAX TRANSPORT VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Medical, Inc.. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K900465. 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 MAX TRANSPORT VENTILATOR?

MAX TRANSPORT VENTILATOR is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Hamilton Medical, Inc.. The 510(k) number is K900465.

When did MAX TRANSPORT VENTILATOR receive FDA 510(k) clearance?

MAX TRANSPORT VENTILATOR received FDA 510(k) clearance on 1990-06-18, under 510(k) number K900465.

Who is the listed applicant for MAX TRANSPORT VENTILATOR?

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

What is the FDA product code for MAX TRANSPORT VENTILATOR?

The FDA product code for MAX TRANSPORT 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 Hamilton Medical, Inc. 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 15 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.

↑