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FDA 510(k)

MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE

K-Number: K883174 · 1988-10-14

ApplicantBaxter Healthcare Corp
Decision Date1988-10-14
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE 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 1988-10-14 under 510(k) number K883174. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE?

MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE is a medical device that received FDA 510(k) clearance on 1988-10-14. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K883174.

When did MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE receive FDA 510(k) clearance?

MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE received FDA 510(k) clearance on 1988-10-14, under 510(k) number K883174.

Who is the listed applicant for MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE?

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 MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE?

The FDA product code for MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE is DQY.

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Other records listing Baxter Healthcare Corp as applicant

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Related Devices (Code: DQY)

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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