RIBBOND(TM)
K-Number: K913040 · 1991-10-07
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Device Summary
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
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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