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FDA 510(k)

ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE

K-Number: K860570 · 1986-03-31

ApplicantParke-Davis Co.
Decision Date1986-03-31
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1986-03-31 under 510(k) number K860570. 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 ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE?

ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1986-03-31. The listed applicant is Parke-Davis Co.. The 510(k) number is K860570.

When did ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE receive FDA 510(k) clearance?

ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE received FDA 510(k) clearance on 1986-03-31, under 510(k) number K860570.

Who is the listed applicant for ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE?

The FDA product code for ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE is KRA.

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Other records listing Parke-Davis Co. 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.

K861725INTRACATH INTRAVENOUS CATHETER PLACEMENT UNITK862119DESERET FLO-THRU INJECTATE TEMPERATURE SENSORK855120ATI DISPOSABLE BIOLOGICAL TEST PACKK860290VIAPIC CENTRAL LINE CATHETERK852192DISPOSABLE STEAM BIOLOGICAL TEST PACKK841967DESERET THERMODILUTION CARDIAC OUTPUT

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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

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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