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FDA 510(k)

SOLO BAND LIGATOR

K-Number: K960020 · 1996-04-01

ApplicantSurcraft, LLC
Decision Date1996-04-01
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SOLO BAND LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Surcraft, LLC. It received FDA 510(k) clearance on 1996-04-01 under 510(k) number K960020. The device is classified under product code FHN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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