COLLAGEN NEUROSPONGE
K-Number: K891993 · 1990-03-23
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Device Summary
Frequently Asked Questions
What is the COLLAGEN NEUROSPONGE?
COLLAGEN NEUROSPONGE is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Vitaphore Corp.. The 510(k) number is K891993.
When did COLLAGEN NEUROSPONGE receive FDA 510(k) clearance?
COLLAGEN NEUROSPONGE received FDA 510(k) clearance on 1990-03-23, under 510(k) number K891993.
Who is the listed applicant for COLLAGEN NEUROSPONGE?
The FDA 510(k) record lists Vitaphore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLAGEN NEUROSPONGE?
The FDA product code for COLLAGEN NEUROSPONGE is HBA.
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 Vitaphore 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.
Related Devices (Code: HBA)
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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