DEPENDABOND
K-Number: K860959 · 1986-03-25
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Device Summary
Frequently Asked Questions
What is the DEPENDABOND?
DEPENDABOND is a medical device that received FDA 510(k) clearance on 1986-03-25. The listed applicant is Ortho Source. The 510(k) number is K860959.
When did DEPENDABOND receive FDA 510(k) clearance?
DEPENDABOND received FDA 510(k) clearance on 1986-03-25, under 510(k) number K860959.
Who is the listed applicant for DEPENDABOND?
The FDA 510(k) record lists Ortho Source as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEPENDABOND?
The FDA product code for DEPENDABOND is DYH.
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 Ortho Source 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: DYH)
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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