Eclipse Blood Collection Set
K-Number: K213690 · 2022-10-26
Device Summary
Frequently Asked Questions
What is the Eclipse Blood Collection Set?
Eclipse Blood Collection Set is a medical device that received FDA 510(k) clearance on 2022-10-26. The listed applicant is Eclipse Medcorp, LLC. The 510(k) number is K213690.
When did Eclipse Blood Collection Set receive FDA 510(k) clearance?
Eclipse Blood Collection Set received FDA 510(k) clearance on 2022-10-26, under 510(k) number K213690.
Who is the listed applicant for Eclipse Blood Collection Set?
The FDA 510(k) record lists Eclipse Medcorp, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eclipse Blood Collection Set?
The FDA product code for Eclipse Blood Collection Set is JKA.
Other records listing Eclipse Medcorp, LLC 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: JKA)
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.