FDA 510(k)

EXTENDED LIFE CAPD TRANSFER SET 5C4444

K-Number: K882498 · 1988-07-13

Decision Date1988-07-13

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

EXTENDED LIFE CAPD TRANSFER SET 5C4444 is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1988-07-13 under 510(k) number K882498. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENDED LIFE CAPD TRANSFER SET 5C4444?

EXTENDED LIFE CAPD TRANSFER SET 5C4444 is a medical device that received FDA 510(k) clearance on 1988-07-13. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K882498.

When did EXTENDED LIFE CAPD TRANSFER SET 5C4444 receive FDA 510(k) clearance?

EXTENDED LIFE CAPD TRANSFER SET 5C4444 received FDA 510(k) clearance on 1988-07-13, under 510(k) number K882498.

Who is the listed applicant for EXTENDED LIFE CAPD TRANSFER SET 5C4444?

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

What is the FDA product code for EXTENDED LIFE CAPD TRANSFER SET 5C4444?

The FDA product code for EXTENDED LIFE CAPD TRANSFER SET 5C4444 is KDJ.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Baxter Healthcare Corp as applicant

K190910PrisMax System Version 2 K163530PrisMax Control Unit K132734NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETS K130245LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFO K123874INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL S K123868INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET

View all 504 devices →

Related Devices (Code: KDJ)

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.