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FDA 510(k)

NEOPHOR-MC

K-Number: K900363 · 1990-04-25

Decision Date1990-04-25
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

NEOPHOR-MC is the device name listed in this FDA 510(k) record. The listed applicant is L.S. Scientific. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K900363. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Unknown.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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