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FDA 510(k)

CARDIOSCAN DOPPLER OPTION

K-Number: K860579 · 1986-06-30

ApplicantInterspec, Inc.
Decision Date1986-06-30
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOSCAN DOPPLER OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Interspec, Inc.. It received FDA 510(k) clearance on 1986-06-30 under 510(k) number K860579. 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 CARDIOSCAN DOPPLER OPTION?

CARDIOSCAN DOPPLER OPTION is a medical device that received FDA 510(k) clearance on 1986-06-30. The listed applicant is Interspec, Inc.. The 510(k) number is K860579.

When did CARDIOSCAN DOPPLER OPTION receive FDA 510(k) clearance?

CARDIOSCAN DOPPLER OPTION received FDA 510(k) clearance on 1986-06-30, under 510(k) number K860579.

Who is the listed applicant for CARDIOSCAN DOPPLER OPTION?

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

What is the FDA product code for CARDIOSCAN DOPPLER OPTION?

The FDA product code for CARDIOSCAN DOPPLER OPTION is JOP.

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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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