FDA 510(k)

NEPHROSS 11F100

K-Number: K790352 · 1979-02-22

Decision Date1979-02-22

Product Code

DecisionUnknown

Device Summary

NEPHROSS 11F100 is the device name listed in this FDA 510(k) record. The listed applicant is Redy Laboratories. It received FDA 510(k) clearance on 1979-02-22 under 510(k) number K790352. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEPHROSS 11F100?

NEPHROSS 11F100 is a medical device that received FDA 510(k) clearance on 1979-02-22. The listed applicant is Redy Laboratories. The 510(k) number is K790352.

When did NEPHROSS 11F100 receive FDA 510(k) clearance?

NEPHROSS 11F100 received FDA 510(k) clearance on 1979-02-22, under 510(k) number K790352.

Who is the listed applicant for NEPHROSS 11F100?

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

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.

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Other records listing Redy Laboratories as applicant

K772290DIALYZER, CAPILATORY, HOLLOW FIBER

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.