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FDA 510(k)

RIBBOND(TM)

K-Number: K913040 · 1991-10-07

ApplicantRibbond, Inc.
Decision Date1991-10-07
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RIBBOND(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Ribbond, Inc.. It received FDA 510(k) clearance on 1991-10-07 under 510(k) number K913040. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIBBOND(TM)?

RIBBOND(TM) is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is Ribbond, Inc.. The 510(k) number is K913040.

When did RIBBOND(TM) receive FDA 510(k) clearance?

RIBBOND(TM) received FDA 510(k) clearance on 1991-10-07, under 510(k) number K913040.

Who is the listed applicant for RIBBOND(TM)?

The FDA 510(k) record lists Ribbond, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIBBOND(TM)?

The FDA product code for RIBBOND(TM) is EBI.

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 Ribbond, Inc. 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: EBI)

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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