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FDA 510(k)

LINA-BAG, MODELS LB-60, LB-100

K-Number: K030422 · 2003-04-14

Decision Date2003-04-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LINA-BAG, MODELS LB-60, LB-100 is the device name listed in this FDA 510(k) record. The listed applicant is Lina Medical Cml Aps. It received FDA 510(k) clearance on 2003-04-14 under 510(k) number K030422. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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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