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FDA 510(k)

MEDCOMP PERITONEAL DIALYSIS CATHETERS

K-Number: K915490 · 1994-02-02

Decision Date1994-02-02
Product CodeFJS
Advisory CommitteeGU
DecisionUnknown

Device Summary

MEDCOMP PERITONEAL DIALYSIS CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1994-02-02 under 510(k) number K915490. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDCOMP PERITONEAL DIALYSIS CATHETERS?

MEDCOMP PERITONEAL DIALYSIS CATHETERS is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Medical Components, Inc.. The 510(k) number is K915490.

When did MEDCOMP PERITONEAL DIALYSIS CATHETERS receive FDA 510(k) clearance?

MEDCOMP PERITONEAL DIALYSIS CATHETERS received FDA 510(k) clearance on 1994-02-02, under 510(k) number K915490.

Who is the listed applicant for MEDCOMP PERITONEAL DIALYSIS CATHETERS?

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

What is the FDA product code for MEDCOMP PERITONEAL DIALYSIS CATHETERS?

The FDA product code for MEDCOMP PERITONEAL DIALYSIS CATHETERS is FJS.

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.

Other records listing Medical Components, Inc. 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.

View all 61 devices →

Related Devices (Code: FJS)

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.

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.

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