LINEAR PLUS
K-Number: K934442 · 1993-10-08
Advertisement
Device Summary
Frequently Asked Questions
What is the LINEAR PLUS?
LINEAR PLUS is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Argosy Electronics. The 510(k) number is K934442.
When did LINEAR PLUS receive FDA 510(k) clearance?
LINEAR PLUS received FDA 510(k) clearance on 1993-10-08, under 510(k) number K934442.
Who is the listed applicant for LINEAR PLUS?
The FDA 510(k) record lists Argosy Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LINEAR PLUS?
The FDA product code for LINEAR PLUS is ESD.
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 Argosy Electronics 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.
Related Devices (Code: ESD)
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.
Advertisement