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FDA 510(k)

5 MHZ TRANSDUCER

K-Number: K872074 · 1987-08-25

ApplicantSonicaid, Inc.
Decision Date1987-08-25
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

5 MHZ TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1987-08-25 under 510(k) number K872074. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5 MHZ TRANSDUCER?

5 MHZ TRANSDUCER is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Sonicaid, Inc.. The 510(k) number is K872074.

When did 5 MHZ TRANSDUCER receive FDA 510(k) clearance?

5 MHZ TRANSDUCER received FDA 510(k) clearance on 1987-08-25, under 510(k) number K872074.

Who is the listed applicant for 5 MHZ TRANSDUCER?

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 5 MHZ TRANSDUCER?

The FDA product code for 5 MHZ TRANSDUCER is JOP.

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Other records listing Sonicaid, Inc. as applicant

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K873673BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONALK863803VASOPULSE(TM)/MODEL 5000K862720VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBESK861237VASOVIEW DUPLEX IMAGING SYSTEMK851102VASOSCREEN IMPEDANCE PLETHYSMOGRAPHK833902VASOSCAN

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Related Devices (Code: JOP)

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.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

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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