OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER
K-Number: K955342 · 1996-06-17
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Device Summary
Frequently Asked Questions
What is the OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER?
OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER is a medical device that received FDA 510(k) clearance on 1996-06-17. The listed applicant is Rashman Corp.. The 510(k) number is K955342.
When did OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER receive FDA 510(k) clearance?
OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER received FDA 510(k) clearance on 1996-06-17, under 510(k) number K955342.
Who is the listed applicant for OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER?
The FDA 510(k) record lists Rashman Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER?
The FDA product code for OMRON, LUMISCOPE, LABTRON, MEDI - SOURCE, BAXTER is DXN.
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.
Related Devices (Code: DXN)
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.
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