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FDA 510(k)

HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT

K-Number: K890277 · 1989-03-10

ApplicantOscor Medical Corp.
Decision Date1989-03-10
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT is the device name listed in this FDA 510(k) record. The listed applicant is Oscor Medical Corp.. It received FDA 510(k) clearance on 1989-03-10 under 510(k) number K890277. 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 HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT?

HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT is a medical device that received FDA 510(k) clearance on 1989-03-10. The listed applicant is Oscor Medical Corp.. The 510(k) number is K890277.

When did HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT receive FDA 510(k) clearance?

HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT received FDA 510(k) clearance on 1989-03-10, under 510(k) number K890277.

Who is the listed applicant for HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT?

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

What is the FDA product code for HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT?

The FDA product code for HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT is DYB.

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Related Devices (Code: DYB)

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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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