B1018 POROUS HA BII-PORE
K-Number: K924288 · 1993-04-14
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Device Summary
Frequently Asked Questions
What is the B1018 POROUS HA BII-PORE?
B1018 POROUS HA BII-PORE is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Bio-Interfaces, Inc.. The 510(k) number is K924288.
When did B1018 POROUS HA BII-PORE receive FDA 510(k) clearance?
B1018 POROUS HA BII-PORE received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924288.
Who is the listed applicant for B1018 POROUS HA BII-PORE?
The FDA 510(k) record lists Bio-Interfaces, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for B1018 POROUS HA BII-PORE?
The FDA product code for B1018 POROUS HA BII-PORE is LYC.
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 Bio-Interfaces, 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: LYC)
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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