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)

SLAVE MONITORS DC109 & VS109

K-Number: K810168 · 1981-02-25

Decision Date1981-02-25
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SLAVE MONITORS DC109 & VS109 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810168. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLAVE MONITORS DC109 & VS109?

SLAVE MONITORS DC109 & VS109 is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Honeywell, Inc.. The 510(k) number is K810168.

When did SLAVE MONITORS DC109 & VS109 receive FDA 510(k) clearance?

SLAVE MONITORS DC109 & VS109 received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810168.

Who is the listed applicant for SLAVE MONITORS DC109 & VS109?

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

What is the FDA product code for SLAVE MONITORS DC109 & VS109?

The FDA product code for SLAVE MONITORS DC109 & VS109 is DXJ.

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 Honeywell, 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 69 devices →

Related Devices (Code: DXJ)

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.

↑