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FDA 510(k)

CAPD STAGED CONNECTOR

K-Number: K845041 · 1985-02-21

ApplicantAbbott Laboratories
Decision Date1985-02-21
Product CodeFKO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAPD STAGED CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K845041. The device is classified under product code FKO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPD STAGED CONNECTOR?

CAPD STAGED CONNECTOR is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Abbott Laboratories. The 510(k) number is K845041.

When did CAPD STAGED CONNECTOR receive FDA 510(k) clearance?

CAPD STAGED CONNECTOR received FDA 510(k) clearance on 1985-02-21, under 510(k) number K845041.

Who is the listed applicant for CAPD STAGED CONNECTOR?

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

What is the FDA product code for CAPD STAGED CONNECTOR?

The FDA product code for CAPD STAGED CONNECTOR is FKO.

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Related Devices (Code: FKO)

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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISCorpak, Inc.K974570PERITONEAL DIALYSIS CATHETER CONNECTORMedigroup, Inc.K910787TITANIUM CONNECTOR (2 PART)Accurate Surgical Instruments Co.K885037AMUKIN 50% - AIRSPRAY(R)Bernard J. Cooney, P.A.K874650PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)Quinton, Inc.K872221DIALY-NATE SET & DIALY-NATE CATHETERGesco Intl., 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.

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