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FDA 510(k)

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS

K-Number: K001059 · 2000-06-30

ApplicantNovex Pharma
Decision Date2000-06-30
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Novex Pharma. It received FDA 510(k) clearance on 2000-06-30 under 510(k) number K001059. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORMOCARB STERILE BICARBONATE RENAL DIALYSIS?

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS is a medical device that received FDA 510(k) clearance on 2000-06-30. The listed applicant is Novex Pharma. The 510(k) number is K001059.

When did NORMOCARB STERILE BICARBONATE RENAL DIALYSIS receive FDA 510(k) clearance?

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS received FDA 510(k) clearance on 2000-06-30, under 510(k) number K001059.

Who is the listed applicant for NORMOCARB STERILE BICARBONATE RENAL DIALYSIS?

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

What is the FDA product code for NORMOCARB STERILE BICARBONATE RENAL DIALYSIS?

The FDA product code for NORMOCARB STERILE BICARBONATE RENAL DIALYSIS is KPO.

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.

Related Devices (Code: KPO)

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.

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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