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FDA 510(k)

HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION

K-Number: K012547 · 2002-01-18

ApplicantDi-Chem, Inc.
Decision Date2002-01-18
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Di-Chem, Inc.. It received FDA 510(k) clearance on 2002-01-18 under 510(k) number K012547. 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 HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION?

HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION is a medical device that received FDA 510(k) clearance on 2002-01-18. The listed applicant is Di-Chem, Inc.. The 510(k) number is K012547.

When did HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION receive FDA 510(k) clearance?

HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION received FDA 510(k) clearance on 2002-01-18, under 510(k) number K012547.

Who is the listed applicant for HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION?

The FDA 510(k) record lists Di-Chem, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION?

The FDA product code for HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION 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.

Other records listing Di-Chem, Inc. as applicant

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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