HAEMONETICS 170 Y INFUSION SET
K-Number: K810365 · 1981-03-31
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Device Summary
Frequently Asked Questions
What is the HAEMONETICS 170 Y INFUSION SET?
HAEMONETICS 170 Y INFUSION SET is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Haemonetics Corp.. The 510(k) number is K810365.
When did HAEMONETICS 170 Y INFUSION SET receive FDA 510(k) clearance?
HAEMONETICS 170 Y INFUSION SET received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810365.
Who is the listed applicant for HAEMONETICS 170 Y INFUSION SET?
The FDA 510(k) record lists Haemonetics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAEMONETICS 170 Y INFUSION SET?
The FDA product code for HAEMONETICS 170 Y INFUSION SET 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 Haemonetics 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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