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FDA 510(k)

PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

K-Number: K910861 · 1991-05-07

ApplicantDaig Corp.
Decision Date1991-05-07
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS INTROD W/SIDEPORT/THREE-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 1991-05-07 under 510(k) number K910861. 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 INTROD W/SIDEPORT/THREE-WAY STOPCOCK?

PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1991-05-07. The listed applicant is Daig Corp.. The 510(k) number is K910861.

When did PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK receive FDA 510(k) clearance?

PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK received FDA 510(k) clearance on 1991-05-07, under 510(k) number K910861.

Who is the listed applicant for PERCUTANEOUS INTROD W/SIDEPORT/THREE-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 INTROD W/SIDEPORT/THREE-WAY STOPCOCK?

The FDA product code for PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK is DYB.

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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.

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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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