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FDA 510(k)

VASOSCREEN IMPEDANCE PLETHYSMOGRAPH

K-Number: K851102 · 1985-05-16

ApplicantSonicaid, Inc.
Decision Date1985-05-16
Product CodeDQB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASOSCREEN IMPEDANCE PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K851102. The device is classified under product code DQB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOSCREEN IMPEDANCE PLETHYSMOGRAPH?

VASOSCREEN IMPEDANCE PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Sonicaid, Inc.. The 510(k) number is K851102.

When did VASOSCREEN IMPEDANCE PLETHYSMOGRAPH receive FDA 510(k) clearance?

VASOSCREEN IMPEDANCE PLETHYSMOGRAPH received FDA 510(k) clearance on 1985-05-16, under 510(k) number K851102.

Who is the listed applicant for VASOSCREEN IMPEDANCE PLETHYSMOGRAPH?

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

What is the FDA product code for VASOSCREEN IMPEDANCE PLETHYSMOGRAPH?

The FDA product code for VASOSCREEN IMPEDANCE PLETHYSMOGRAPH is DQB.

Related Clinical Trials

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.

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Other records listing Sonicaid, 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.

K873673BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONALK8720745 MHZ TRANSDUCERK863803VASOPULSE(TM)/MODEL 5000K862720VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBESK861237VASOVIEW DUPLEX IMAGING SYSTEMK833902VASOSCAN

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Related Devices (Code: DQB)

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.

K822873DEVETHERMEko Scann ABK772093IMPEDANCE RHEOGRAPHDynatech Research & Development Co.

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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