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FDA 510(k)

PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK

K-Number: K870374 · 1987-03-18

ApplicantDaig Corp.
Decision Date1987-03-18
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1987-03-18 under 510(k) number K870374. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 63 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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