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FDA 510(k)

RIGHT ATRIAL CATHETER KITS

K-Number: K920331 · 1992-04-22

ApplicantAkcess Medical Products, Inc.
Decision Date1992-04-22
Product CodeDQY
Advisory CommitteeCV
DecisionUnknown

Device Summary

RIGHT ATRIAL CATHETER KITS is the device name listed in this FDA 510(k) record. The listed applicant is Akcess Medical Products, Inc.. It received FDA 510(k) clearance on 1992-04-22 under 510(k) number K920331. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RIGHT ATRIAL CATHETER KITS?

RIGHT ATRIAL CATHETER KITS is a medical device that received FDA 510(k) clearance on 1992-04-22. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K920331.

When did RIGHT ATRIAL CATHETER KITS receive FDA 510(k) clearance?

RIGHT ATRIAL CATHETER KITS received FDA 510(k) clearance on 1992-04-22, under 510(k) number K920331.

Who is the listed applicant for RIGHT ATRIAL CATHETER KITS?

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

What is the FDA product code for RIGHT ATRIAL CATHETER KITS?

The FDA product code for RIGHT ATRIAL CATHETER KITS is DQY.

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Other records listing Akcess Medical Products, 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.

K926374SILICONE CATHETER REPAIR KITSK925819AKCESS0CATH KITK925818AKCESS-CATHK930630RIGHT ATRIAL CATHETERK931120COAXIAL ACUTE CATHETERK920634SPLITTABLE SHEATH INTRODUCER SET

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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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