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)

ACUTE RENAL DIALYSIS TRAY

K-Number: K790353 · 1979-04-20

ApplicantArgon Medical Corp.
Decision Date1979-04-20
Product CodeFKG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACUTE RENAL DIALYSIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1979-04-20 under 510(k) number K790353. The device is classified under product code FKG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUTE RENAL DIALYSIS TRAY?

ACUTE RENAL DIALYSIS TRAY is a medical device that received FDA 510(k) clearance on 1979-04-20. The listed applicant is Argon Medical Corp.. The 510(k) number is K790353.

When did ACUTE RENAL DIALYSIS TRAY receive FDA 510(k) clearance?

ACUTE RENAL DIALYSIS TRAY received FDA 510(k) clearance on 1979-04-20, under 510(k) number K790353.

Who is the listed applicant for ACUTE RENAL DIALYSIS TRAY?

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

What is the FDA product code for ACUTE RENAL DIALYSIS TRAY?

The FDA product code for ACUTE RENAL DIALYSIS TRAY is FKG.

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

Other records listing Argon Medical Corp. 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.

K904994CLOSED SYSTEM FLUSH SETK895511CATHETER BALLOON DILATOR PRESSURE GAUGEK894157OBTURATORK891022INTRODUCER FOR PTCA GUIDING CATHETERSK884375TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETERK882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE

View all 27 devices →

Related Devices (Code: FKG)

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.

K925469JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KITJ.J. Skinner, Inc.K871630KITS AND TRAYS FOR DIALYSIS USEDove Medical SuppliesK833780CAPD PREP KITProfessional Dialysis ProductsK802361DIALYIS START CARE KITMed-Pak Corp.K792207PERIDIAL PERITONEAL DIALYSIS TRAYCutter Laboratories, Inc.

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.

↑