LIFEPORT(R) 7 INCH CONTINUOUS INFUSION W/Y-SITE
K-Number: K870582 · 1987-04-23
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Device Summary
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.
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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