INTRODUCER, PERCUTANEOUS
K-Number: K870907 · 1987-04-09
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Device Summary
Frequently Asked Questions
What is the INTRODUCER, PERCUTANEOUS?
INTRODUCER, PERCUTANEOUS is a medical device that received FDA 510(k) clearance on 1987-04-09. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K870907.
When did INTRODUCER, PERCUTANEOUS receive FDA 510(k) clearance?
INTRODUCER, PERCUTANEOUS received FDA 510(k) clearance on 1987-04-09, under 510(k) number K870907.
Who is the listed applicant for INTRODUCER, PERCUTANEOUS?
The FDA 510(k) record lists Med Fusion Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRODUCER, PERCUTANEOUS?
The FDA product code for INTRODUCER, PERCUTANEOUS is DYB.
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 Med Fusion Systems, 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: DYB)
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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