INFUSION MANIFOLD
K-Number: K873852 · 1987-11-23
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Device Summary
Frequently Asked Questions
What is the INFUSION MANIFOLD?
INFUSION MANIFOLD is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K873852.
When did INFUSION MANIFOLD receive FDA 510(k) clearance?
INFUSION MANIFOLD received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873852.
Who is the listed applicant for INFUSION MANIFOLD?
The FDA 510(k) record lists Advanced Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION MANIFOLD?
The FDA product code for INFUSION MANIFOLD is FPK.
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 Advanced Surgical Products, 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: FPK)
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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