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FDA 510(k)

LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH.

K-Number: K880305 · 1988-04-26

Decision Date1988-04-26
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. 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 1988-04-26 under 510(k) number K880305. 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 LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH.?

LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. is a medical device that received FDA 510(k) clearance on 1988-04-26. The listed applicant is Strato Medical Corp.. The 510(k) number is K880305.

When did LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. receive FDA 510(k) clearance?

LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. received FDA 510(k) clearance on 1988-04-26, under 510(k) number K880305.

Who is the listed applicant for LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH.?

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 LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH.?

The FDA product code for LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. 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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