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FDA 510(k)

7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T

K-Number: K860494 · 1986-03-26

ApplicantAusonics Pty , Ltd.
Decision Date1986-03-26
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T is the device name listed in this FDA 510(k) record. The listed applicant is Ausonics Pty , Ltd.. It received FDA 510(k) clearance on 1986-03-26 under 510(k) number K860494. 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 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T?

7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T is a medical device that received FDA 510(k) clearance on 1986-03-26. The listed applicant is Ausonics Pty , Ltd.. The 510(k) number is K860494.

When did 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T receive FDA 510(k) clearance?

7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T received FDA 510(k) clearance on 1986-03-26, under 510(k) number K860494.

Who is the listed applicant for 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T?

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

What is the FDA product code for 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T?

The FDA product code for 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T is ITX.

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Other records listing Ausonics Pty , Ltd. 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.

K933916AUSONICS OPUS 2 REALTIME ULTRASOUND SCANNERK915715CINE RECALL FUNCTION/OPUS 1 REAL TIME SCANNERK920307AUSONICS OPUS 1 SYSTEM, ANNULAR ARRAY OPTIONK905488DOPPLER UPGRADE FOR AUSONICS OPUS 1 REAL TIME SCANK9027287.5 MHZ BI PLANE RECTAL PROBE (P/N: 041-815)K896714AUSONICS 5000

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Related Devices (Code: ITX)

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.

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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