VOSS GRAFT MARKER
K-Number: K895369 · 1989-09-27
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Device Summary
Frequently Asked Questions
What is the VOSS GRAFT MARKER?
VOSS GRAFT MARKER is a medical device that received FDA 510(k) clearance on 1989-09-27. The listed applicant is Voss Medical Products. The 510(k) number is K895369.
When did VOSS GRAFT MARKER receive FDA 510(k) clearance?
VOSS GRAFT MARKER received FDA 510(k) clearance on 1989-09-27, under 510(k) number K895369.
Who is the listed applicant for VOSS GRAFT MARKER?
The FDA 510(k) record lists Voss Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOSS GRAFT MARKER?
The FDA product code for VOSS GRAFT MARKER is KPK.
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 Voss Medical Products 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: KPK)
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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