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FDA 510(k)

MODIFIED FLOCATH PULMONARY ARTERY CATHETER

K-Number: K901733 · 1990-07-16

ApplicantCardio Metrics, Inc.
Decision Date1990-07-16
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED FLOCATH PULMONARY ARTERY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Metrics, Inc.. It received FDA 510(k) clearance on 1990-07-16 under 510(k) number K901733. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED FLOCATH PULMONARY ARTERY CATHETER?

MODIFIED FLOCATH PULMONARY ARTERY CATHETER is a medical device that received FDA 510(k) clearance on 1990-07-16. The listed applicant is Cardio Metrics, Inc.. The 510(k) number is K901733.

When did MODIFIED FLOCATH PULMONARY ARTERY CATHETER receive FDA 510(k) clearance?

MODIFIED FLOCATH PULMONARY ARTERY CATHETER received FDA 510(k) clearance on 1990-07-16, under 510(k) number K901733.

Who is the listed applicant for MODIFIED FLOCATH PULMONARY ARTERY CATHETER?

The FDA 510(k) record lists Cardio Metrics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED FLOCATH PULMONARY ARTERY CATHETER?

The FDA product code for MODIFIED FLOCATH PULMONARY ARTERY CATHETER is DPW.

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Other records listing Cardio Metrics, Inc. 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.

K972762CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRESK965140CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEMK951567CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIREK961777ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404K955551CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404K954913CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)

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Related Devices (Code: DPW)

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.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, Inc.

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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