Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD

K-Number: K852955 · 1986-02-05

ApplicantRenalchem, Inc.
Decision Date1986-02-05
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD is the device name listed in this FDA 510(k) record. The listed applicant is Renalchem, Inc.. It received FDA 510(k) clearance on 1986-02-05 under 510(k) number K852955. 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 HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD?

HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD is a medical device that received FDA 510(k) clearance on 1986-02-05. The listed applicant is Renalchem, Inc.. The 510(k) number is K852955.

When did HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD receive FDA 510(k) clearance?

HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD received FDA 510(k) clearance on 1986-02-05, under 510(k) number K852955.

Who is the listed applicant for HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD?

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

What is the FDA product code for HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD?

The FDA product code for HEMOD CONCE OF VAR FORMU & LIPUID HEMOD CONCE ADD 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K260799Nipro Dry Acid Concentrate MixerNipro Technical Solutions, IncoporatedK253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)Fresenius Medical Care Renal Therapies Group, LLCK252180Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby Dialysate RFP-403 (RFP-403-G); Bicarby Dialysate RFP-453 (RFP-453-W); Bicarby Dialysate RFP-453 (RFP-453-G); Bicarby Dialysate RFP-454 (RFP-454-W); Bicarby Dialysate RFP-454 (RFP-454-G); Bicarby Dialysate RFP-456 (RFP-456-W)Fresenius Medical Care Renal Therapies Group, LLCK243786Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G)Fresenius Medical Care Renal Therapies Group, LLCK240920HemoCare Bicarbonate Concentrate Set (BCS)Deka Research and DevelopmentK233950pureFLOW 402 (F00012067); pureFLOW 406 (F00012068); pureFLOW 401 (F00012069); pureFLOW 400 (F00012070)Fresenius Medical Care Renal Therapies Group, LLC

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.

↑