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FDA 510(k)

RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES

K-Number: K860699 · 1986-04-02

ApplicantIntracath, Inc.
Decision Date1986-04-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Intracath, Inc.. It received FDA 510(k) clearance on 1986-04-02 under 510(k) number K860699. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES?

RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES is a medical device that received FDA 510(k) clearance on 1986-04-02. The listed applicant is Intracath, Inc.. The 510(k) number is K860699.

When did RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES receive FDA 510(k) clearance?

RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES received FDA 510(k) clearance on 1986-04-02, under 510(k) number K860699.

Who is the listed applicant for RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES?

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

What is the FDA product code for RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES?

The FDA product code for RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES is DQY.

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Related Devices (Code: DQY)

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.

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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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