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FDA 510(k)

ULTRASOUND TRANSMISSION GEL

K-Number: K905545 · 1991-03-29

ApplicantArbo Medical, Inc.
Decision Date1991-03-29
Product CodeJOT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRASOUND TRANSMISSION GEL is the device name listed in this FDA 510(k) record. The listed applicant is Arbo Medical, Inc.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K905545. The device is classified under product code JOT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASOUND TRANSMISSION GEL?

ULTRASOUND TRANSMISSION GEL is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Arbo Medical, Inc.. The 510(k) number is K905545.

When did ULTRASOUND TRANSMISSION GEL receive FDA 510(k) clearance?

ULTRASOUND TRANSMISSION GEL received FDA 510(k) clearance on 1991-03-29, under 510(k) number K905545.

Who is the listed applicant for ULTRASOUND TRANSMISSION GEL?

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

What is the FDA product code for ULTRASOUND TRANSMISSION GEL?

The FDA product code for ULTRASOUND TRANSMISSION GEL is JOT.

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Other records listing Arbo Medical, 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.

K940323ARBO DIAGNOSTIC ECG PATIENT CABLES & LEADWIRES ARBO SHIELDED MULTI-LEAD CABLE & LEAD SYSTEMK935437ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODESK942905DISPOSABLE TEMPERATURE PROBE COVERK940302ARBO MONITRING SAFETY CABLE & LEAD WIRE SYSTEMS/ARBO UNSHEILDED SAFETY CABLE & LEAD SYSTEMK940322ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIREK935246ARBO H49P, H59P DISPOSABLE MONITORING ELECTRODES

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Related Devices (Code: JOT)

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.

K923647RFG-DGP DISPOSABLE GROUNDING PADSRadionics, Inc.K904418ULTRASOUND COUPLING GELGeno LaboratoriesK901217TRIA-SONIC ULTRA SOUND TRANSMISSION GELH & P Industries, Inc.K894490STERILE ULTRASOUND TRANSMISSION GELSwedish Trade Council USAK884503ULTRASONIC TRANSMISSION GELHerbert Stanley Co.K872519STERILIZED OMNI GELEcho Ultrasound

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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