AUTO-BAND LIGATOR
K-Number: K031236 · 2003-11-14
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Device Summary
Frequently Asked Questions
What is the AUTO-BAND LIGATOR?
AUTO-BAND LIGATOR is a medical device that received FDA 510(k) clearance on 2003-11-14. The listed applicant is Scandimed. A.S.. The 510(k) number is K031236.
When did AUTO-BAND LIGATOR receive FDA 510(k) clearance?
AUTO-BAND LIGATOR received FDA 510(k) clearance on 2003-11-14, under 510(k) number K031236.
Who is the listed applicant for AUTO-BAND LIGATOR?
The FDA 510(k) record lists Scandimed. A.S. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTO-BAND LIGATOR?
The FDA product code for AUTO-BAND LIGATOR is MND.
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 Scandimed. A.S. 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: MND)
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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