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FDA 510(k)

DAIG FAST CATH(TM) INTRODUCER, MODIFICATION

K-Number: K914090 · 1991-10-28

ApplicantDaig Corp.
Decision Date1991-10-28
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAIG FAST CATH(TM) INTRODUCER, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1991-10-28 under 510(k) number K914090. 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 DAIG FAST CATH(TM) INTRODUCER, MODIFICATION?

DAIG FAST CATH(TM) INTRODUCER, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-10-28. The listed applicant is Daig Corp.. The 510(k) number is K914090.

When did DAIG FAST CATH(TM) INTRODUCER, MODIFICATION receive FDA 510(k) clearance?

DAIG FAST CATH(TM) INTRODUCER, MODIFICATION received FDA 510(k) clearance on 1991-10-28, under 510(k) number K914090.

Who is the listed applicant for DAIG FAST CATH(TM) INTRODUCER, MODIFICATION?

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 DAIG FAST CATH(TM) INTRODUCER, MODIFICATION?

The FDA product code for DAIG FAST CATH(TM) INTRODUCER, MODIFICATION 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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