FDA 510(k)

CAPD PREP KIT

K-Number: K833780 · 1984-02-09

Decision Date1984-02-09

Product CodeFKG

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CAPD PREP KIT is the device name listed in this FDA 510(k) record. The listed applicant is Professional Dialysis Products. It received FDA 510(k) clearance on 1984-02-09 under 510(k) number K833780. 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 CAPD PREP KIT?

CAPD PREP KIT is a medical device that received FDA 510(k) clearance on 1984-02-09. The listed applicant is Professional Dialysis Products. The 510(k) number is K833780.

When did CAPD PREP KIT receive FDA 510(k) clearance?

CAPD PREP KIT received FDA 510(k) clearance on 1984-02-09, under 510(k) number K833780.

Who is the listed applicant for CAPD PREP KIT?

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

What is the FDA product code for CAPD PREP KIT?

The FDA product code for CAPD PREP KIT is FKG.

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 Supplies K802361DIALYIS START CARE KITMed-Pak Corp.K792207PERIDIAL PERITONEAL DIALYSIS TRAYCutter Laboratories, Inc.K790353ACUTE RENAL DIALYSIS TRAYArgon Medical Corp.

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.