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FDA 510(k)

STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR

K-Number: K885247 · 1989-03-10

ApplicantBaxter Healthcare Corp
Decision Date1989-03-10
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1989-03-10 under 510(k) number K885247. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR?

STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR is a medical device that received FDA 510(k) clearance on 1989-03-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K885247.

When did STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR receive FDA 510(k) clearance?

STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR received FDA 510(k) clearance on 1989-03-10, under 510(k) number K885247.

Who is the listed applicant for STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR?

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

What is the FDA product code for STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR?

The FDA product code for STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR is LIT.

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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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