SOLO BAND LIGATOR
K-Number: K960020 · 1996-04-01
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Device Summary
Frequently Asked Questions
What is the SOLO BAND LIGATOR?
SOLO BAND LIGATOR is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Surcraft, LLC. The 510(k) number is K960020.
When did SOLO BAND LIGATOR receive FDA 510(k) clearance?
SOLO BAND LIGATOR received FDA 510(k) clearance on 1996-04-01, under 510(k) number K960020.
Who is the listed applicant for SOLO BAND LIGATOR?
The FDA 510(k) record lists Surcraft, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLO BAND LIGATOR?
The FDA product code for SOLO BAND LIGATOR is FHN.
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: FHN)
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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