PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK
K-Number: K870374 · 1987-03-18
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Device Summary
Frequently Asked Questions
What is the PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK?
PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1987-03-18. The listed applicant is Daig Corp.. The 510(k) number is K870374.
When did PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK receive FDA 510(k) clearance?
PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK received FDA 510(k) clearance on 1987-03-18, under 510(k) number K870374.
Who is the listed applicant for PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK?
The FDA 510(k) record lists Daig Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK?
The FDA product code for PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK 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 Daig 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: 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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