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FDA 510(k)

PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM

K-Number: K871912 · 1988-02-18

ApplicantElectro-Diagnostic Instruments
Decision Date1988-02-18
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Diagnostic Instruments. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K871912. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM?

PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Electro-Diagnostic Instruments. The 510(k) number is K871912.

When did PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM receive FDA 510(k) clearance?

PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM received FDA 510(k) clearance on 1988-02-18, under 510(k) number K871912.

Who is the listed applicant for PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM?

The FDA 510(k) record lists Electro-Diagnostic Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM?

The FDA product code for PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM is DPT.

Related Clinical Trials

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Other records listing Electro-Diagnostic Instruments 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.

K932438MODEL IPM-1 IMPEDANCE PULSE MONITORK862714BILATERAL IMPEDANCE PLETHYSMOGRAPH, BIP(TM)K822455VASOGRAPH, MODEL MV-2

Related Devices (Code: DPT)

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.

K233076Laser Speckle Imaging System (RFLSI CZW)Rwd Life Science Co., Ltd.K163339SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.0Spectralmd, Inc.K152749moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser Doppler imager, moorLDI2-VR Visible Red laser Doppler imagerMoor Instruments, Ltd.K124049DEEPVIEW DIGITAL VIDEO PHYSIOLOGICAL PORTABLE IMAGING SYSTEMSpectralmd, Inc.K123216AIMAGO EASYLDI MICROCIRCULATION CAMERA (STAND PLUS CAMERA ARM), AIMAGO EASY LDI STAND, INCLUDING 4-WHEELED STAND BASE ANAimago SAK122943MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGERMoor Instruments, Ltd.

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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