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FDA 510(k)

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER

K-Number: K900155 · 1990-10-05

ApplicantInterspec, Inc.
Decision Date1990-10-05
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Interspec, Inc.. It received FDA 510(k) clearance on 1990-10-05 under 510(k) number K900155. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER?

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER is a medical device that received FDA 510(k) clearance on 1990-10-05. The listed applicant is Interspec, Inc.. The 510(k) number is K900155.

When did INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER receive FDA 510(k) clearance?

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER received FDA 510(k) clearance on 1990-10-05, under 510(k) number K900155.

Who is the listed applicant for INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER?

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 INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER?

The FDA product code for INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER is ITX.

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Other records listing Interspec, Inc. as applicant

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Related Devices (Code: ITX)

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K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, Inc.

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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