DUAL LUER LOCK CAP, MODEL 2C6250
K-Number: K101385 · 2010-06-22
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Device Summary
Frequently Asked Questions
What is the DUAL LUER LOCK CAP, MODEL 2C6250?
DUAL LUER LOCK CAP, MODEL 2C6250 is a medical device that received FDA 510(k) clearance on 2010-06-22. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K101385.
When did DUAL LUER LOCK CAP, MODEL 2C6250 receive FDA 510(k) clearance?
DUAL LUER LOCK CAP, MODEL 2C6250 received FDA 510(k) clearance on 2010-06-22, under 510(k) number K101385.
Who is the listed applicant for DUAL LUER LOCK CAP, MODEL 2C6250?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUAL LUER LOCK CAP, MODEL 2C6250?
The FDA product code for DUAL LUER LOCK CAP, MODEL 2C6250 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 Baxter Healthcare 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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