NEOPHOR-MC
K-Number: K900363 · 1990-04-25
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Device Summary
Frequently Asked Questions
What is the NEOPHOR-MC?
NEOPHOR-MC is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is L.S. Scientific. The 510(k) number is K900363.
When did NEOPHOR-MC receive FDA 510(k) clearance?
NEOPHOR-MC received FDA 510(k) clearance on 1990-04-25, under 510(k) number K900363.
Who is the listed applicant for NEOPHOR-MC?
The FDA 510(k) record lists L.S. Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEOPHOR-MC?
The FDA product code for NEOPHOR-MC is EGJ.
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 L.S. Scientific 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: EGJ)
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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