LINA-BAG, MODELS LB-60, LB-100
K-Number: K030422 · 2003-04-14
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Device Summary
Frequently Asked Questions
What is the LINA-BAG, MODELS LB-60, LB-100?
LINA-BAG, MODELS LB-60, LB-100 is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Lina Medical Cml Aps. The 510(k) number is K030422.
When did LINA-BAG, MODELS LB-60, LB-100 receive FDA 510(k) clearance?
LINA-BAG, MODELS LB-60, LB-100 received FDA 510(k) clearance on 2003-04-14, under 510(k) number K030422.
Who is the listed applicant for LINA-BAG, MODELS LB-60, LB-100?
The FDA 510(k) record lists Lina Medical Cml Aps as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LINA-BAG, MODELS LB-60, LB-100?
The FDA product code for LINA-BAG, MODELS LB-60, LB-100 is GCJ.
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.
Related Devices (Code: GCJ)
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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