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FDA 510(k)

SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000

K-Number: K901061 · 1990-05-22

Decision Date1990-05-22
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000 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 1990-05-22 under 510(k) number K901061. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000?

SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000 is a medical device that received FDA 510(k) clearance on 1990-05-22. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K901061.

When did SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000 receive FDA 510(k) clearance?

SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000 received FDA 510(k) clearance on 1990-05-22, under 510(k) number K901061.

Who is the listed applicant for SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000?

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 SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000?

The FDA product code for SUB-CLAVIAN CATHETERS SLSC 1300, 1500 AND 2000 is LFJ.

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 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.

View all 36 devices →

Related Devices (Code: LFJ)

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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