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FDA 510(k)

NEPHROSS I.Q. ALLEGO

K-Number: K882213 · 1988-06-28

ApplicantOrganon Teknika Corp.
Decision Date1988-06-28
Product CodeFJI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEPHROSS I.Q. ALLEGO is the device name listed in this FDA 510(k) record. The listed applicant is Organon Teknika Corp.. It received FDA 510(k) clearance on 1988-06-28 under 510(k) number K882213. The device is classified under product code FJI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEPHROSS I.Q. ALLEGO?

NEPHROSS I.Q. ALLEGO is a medical device that received FDA 510(k) clearance on 1988-06-28. The listed applicant is Organon Teknika Corp.. The 510(k) number is K882213.

When did NEPHROSS I.Q. ALLEGO receive FDA 510(k) clearance?

NEPHROSS I.Q. ALLEGO received FDA 510(k) clearance on 1988-06-28, under 510(k) number K882213.

Who is the listed applicant for NEPHROSS I.Q. ALLEGO?

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

What is the FDA product code for NEPHROSS I.Q. ALLEGO?

The FDA product code for NEPHROSS I.Q. ALLEGO is FJI.

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Related Devices (Code: FJI)

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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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