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FDA 510(k)

LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE

K-Number: K870582 · 1987-04-23

Decision Date1987-04-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE 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 1987-04-23 under 510(k) number K870582. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE?

LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE is a medical device that received FDA 510(k) clearance on 1987-04-23. The listed applicant is Strato Medical Corp.. The 510(k) number is K870582.

When did LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE receive FDA 510(k) clearance?

LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE received FDA 510(k) clearance on 1987-04-23, under 510(k) number K870582.

Who is the listed applicant for LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE?

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(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE?

The FDA product code for LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE is FPA.

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: FPA)

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

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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