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FDA 510(k)

NEPHROSS ALLEGRO H.F.

K-Number: K844748 · 1985-01-22

ApplicantOrganon Teknika Corp.
Decision Date1985-01-22
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEPHROSS ALLEGRO H.F. 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 1985-01-22 under 510(k) number K844748. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEPHROSS ALLEGRO H.F.?

NEPHROSS ALLEGRO H.F. is a medical device that received FDA 510(k) clearance on 1985-01-22. The listed applicant is Organon Teknika Corp.. The 510(k) number is K844748.

When did NEPHROSS ALLEGRO H.F. receive FDA 510(k) clearance?

NEPHROSS ALLEGRO H.F. received FDA 510(k) clearance on 1985-01-22, under 510(k) number K844748.

Who is the listed applicant for NEPHROSS ALLEGRO H.F.?

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 ALLEGRO H.F.?

The FDA product code for NEPHROSS ALLEGRO H.F. is FKQ.

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Other records listing Organon Teknika Corp. as applicant

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Related Devices (Code: FKQ)

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.

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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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