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FDA 510(k)

BIONOR TRANSPORTMEDIUM

K-Number: K925450 · 1993-06-25

ApplicantSkoug Research Corp.
Decision Date1993-06-25
Product CodeJSL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BIONOR TRANSPORTMEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Skoug Research Corp.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K925450. The device is classified under product code JSL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIONOR TRANSPORTMEDIUM?

BIONOR TRANSPORTMEDIUM is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is Skoug Research Corp.. The 510(k) number is K925450.

When did BIONOR TRANSPORTMEDIUM receive FDA 510(k) clearance?

BIONOR TRANSPORTMEDIUM received FDA 510(k) clearance on 1993-06-25, under 510(k) number K925450.

Who is the listed applicant for BIONOR TRANSPORTMEDIUM?

The FDA 510(k) record lists Skoug Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIONOR TRANSPORTMEDIUM?

The FDA product code for BIONOR TRANSPORTMEDIUM is JSL.

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Related Devices (Code: JSL)

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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.

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