FDA 510(k)

LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER

K-Number: K870886 · 1987-05-06

Decision Date1987-05-06

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER 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 1987-05-06 under 510(k) number K870886. 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 VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER?

LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is Strato Medical Corp.. The 510(k) number is K870886.

When did LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER receive FDA 510(k) clearance?

LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER received FDA 510(k) clearance on 1987-05-06, under 510(k) number K870886.

Who is the listed applicant for LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER?

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 VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER?

The FDA product code for LIFEPORT VASCULAR ACCESS SYSTEM W/0.76 MM CATHETER is LJT.

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Other records listing Strato Medical Corp. as applicant

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Related Devices (Code: LJT)

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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.