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FDA 510(k)

LIFE-PORT IMPLANTABLE VASCULAR ACCESS

K-Number: K853827 · 1986-11-13

Decision Date1986-11-13
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFE-PORT IMPLANTABLE VASCULAR ACCESS is the device name listed in this FDA 510(k) record. The listed applicant is Strato Medical Corp.. It received FDA 510(k) clearance on 1986-11-13 under 510(k) number K853827. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE-PORT IMPLANTABLE VASCULAR ACCESS?

LIFE-PORT IMPLANTABLE VASCULAR ACCESS is a medical device that received FDA 510(k) clearance on 1986-11-13. The listed applicant is Strato Medical Corp.. The 510(k) number is K853827.

When did LIFE-PORT IMPLANTABLE VASCULAR ACCESS receive FDA 510(k) clearance?

LIFE-PORT IMPLANTABLE VASCULAR ACCESS received FDA 510(k) clearance on 1986-11-13, under 510(k) number K853827.

Who is the listed applicant for LIFE-PORT IMPLANTABLE VASCULAR ACCESS?

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

What is the FDA product code for LIFE-PORT IMPLANTABLE VASCULAR ACCESS?

The FDA product code for LIFE-PORT IMPLANTABLE VASCULAR ACCESS is LJT.

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 Strato Medical Corp. 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 45 devices →

Related Devices (Code: LJT)

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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