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FDA 510(k)

SHUNT CONNECTORS

K-Number: K893679 · 1989-07-24

ApplicantAkcess Medical Products, Inc.
Decision Date1989-07-24
Product CodeFJQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SHUNT CONNECTORS 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 1989-07-24 under 510(k) number K893679. The device is classified under product code FJQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHUNT CONNECTORS?

SHUNT CONNECTORS is a medical device that received FDA 510(k) clearance on 1989-07-24. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K893679.

When did SHUNT CONNECTORS receive FDA 510(k) clearance?

SHUNT CONNECTORS received FDA 510(k) clearance on 1989-07-24, under 510(k) number K893679.

Who is the listed applicant for SHUNT CONNECTORS?

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 SHUNT CONNECTORS?

The FDA product code for SHUNT CONNECTORS is FJQ.

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Other records listing Akcess Medical Products, Inc. as applicant

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

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Related Devices (Code: FJQ)

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.

K771422PATIENT BY-PASSQuinton, Inc.K771429DISP. TEFLON CONNHCTORQuinton, 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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