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FDA 510(k)

VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION

K-Number: K896819 · 1990-01-19

ApplicantBaxter Healthcare Corp
Decision Date1990-01-19
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION 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 1990-01-19 under 510(k) number K896819. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION?

VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K896819.

When did VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION receive FDA 510(k) clearance?

VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION received FDA 510(k) clearance on 1990-01-19, under 510(k) number K896819.

Who is the listed applicant for VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION?

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 VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION?

The FDA product code for VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION is KRA.

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Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

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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