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FDA 510(k)

PERIFLUX PF-2

K-Number: K844631 · 1985-02-20

ApplicantMedex, Inc.
Decision Date1985-02-20
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERIFLUX PF-2 is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1985-02-20 under 510(k) number K844631. 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 PERIFLUX PF-2?

PERIFLUX PF-2 is a medical device that received FDA 510(k) clearance on 1985-02-20. The listed applicant is Medex, Inc.. The 510(k) number is K844631.

When did PERIFLUX PF-2 receive FDA 510(k) clearance?

PERIFLUX PF-2 received FDA 510(k) clearance on 1985-02-20, under 510(k) number K844631.

Who is the listed applicant for PERIFLUX PF-2?

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

What is the FDA product code for PERIFLUX PF-2?

The FDA product code for PERIFLUX PF-2 is DPW.

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Related Devices (Code: DPW)

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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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