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FDA 510(k)

SUBCLAVIAN INTRODUCER SET

K-Number: K902251 · 1990-07-31

Decision Date1990-07-31
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUBCLAVIAN INTRODUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Infusaid Corp.. It received FDA 510(k) clearance on 1990-07-31 under 510(k) number K902251. 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 SUBCLAVIAN INTRODUCER SET?

SUBCLAVIAN INTRODUCER SET is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Infusaid Corp.. The 510(k) number is K902251.

When did SUBCLAVIAN INTRODUCER SET receive FDA 510(k) clearance?

SUBCLAVIAN INTRODUCER SET received FDA 510(k) clearance on 1990-07-31, under 510(k) number K902251.

Who is the listed applicant for SUBCLAVIAN INTRODUCER SET?

The FDA 510(k) record lists Infusaid Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUBCLAVIAN INTRODUCER SET?

The FDA product code for SUBCLAVIAN INTRODUCER SET 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 Infusaid 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 8 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

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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