FDA 510(k)

MSI-DIFF PLUS

K-Number: K880270 · 1988-03-01

Decision Date1988-03-01

Product CodeJPK

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

MSI-DIFF PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialties, Inc.. It received FDA 510(k) clearance on 1988-03-01 under 510(k) number K880270. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSI-DIFF PLUS?

MSI-DIFF PLUS is a medical device that received FDA 510(k) clearance on 1988-03-01. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K880270.

When did MSI-DIFF PLUS receive FDA 510(k) clearance?

MSI-DIFF PLUS received FDA 510(k) clearance on 1988-03-01, under 510(k) number K880270.

Who is the listed applicant for MSI-DIFF PLUS?

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

What is the FDA product code for MSI-DIFF PLUS?

The FDA product code for MSI-DIFF PLUS is JPK.

Other records listing Medical Specialties, 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.

K946201STAND, INFUSION K931947CHECKPOINT K926095REFRACTROL-SP K924926MSI-HCT K896566MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE K883851MSI-CAL 8

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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.