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FDA 510(k)

SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR

K-Number: K981669 · 1998-06-04

Decision Date1998-06-04
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1998-06-04 under 510(k) number K981669. 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 SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR?

SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR is a medical device that received FDA 510(k) clearance on 1998-06-04. The listed applicant is Boston Scientific Corp. The 510(k) number is K981669.

When did SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR receive FDA 510(k) clearance?

SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR received FDA 510(k) clearance on 1998-06-04, under 510(k) number K981669.

Who is the listed applicant for SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR?

The FDA product code for SPEEDBAND SUPERVIEW MULTIPLE 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.

Other records listing Boston Scientific Corp 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.

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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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