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FDA 510(k)

LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER

K-Number: K922034 · 1993-05-18

ApplicantTitronics Medical Instruments, Inc.
Decision Date1993-05-18
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER is the device name listed in this FDA 510(k) record. The listed applicant is Titronics Medical Instruments, Inc.. It received FDA 510(k) clearance on 1993-05-18 under 510(k) number K922034. 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 LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER?

LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER is a medical device that received FDA 510(k) clearance on 1993-05-18. The listed applicant is Titronics Medical Instruments, Inc.. The 510(k) number is K922034.

When did LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER receive FDA 510(k) clearance?

LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER received FDA 510(k) clearance on 1993-05-18, under 510(k) number K922034.

Who is the listed applicant for LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER?

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

What is the FDA product code for LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER?

The FDA product code for LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER is DPW.

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Other records listing Titronics Medical Instruments, Inc. as applicant

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Official Source

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