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FDA 510(k)

TRIA-SONIC ULTRA SOUND TRANSMISSION GEL

K-Number: K901217 · 1990-06-22

ApplicantH & P Industries, Inc.
Decision Date1990-06-22
Product CodeJOT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIA-SONIC ULTRA SOUND TRANSMISSION GEL is the device name listed in this FDA 510(k) record. The listed applicant is H & P Industries, Inc.. It received FDA 510(k) clearance on 1990-06-22 under 510(k) number K901217. 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 TRIA-SONIC ULTRA SOUND TRANSMISSION GEL?

TRIA-SONIC ULTRA SOUND TRANSMISSION GEL is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is H & P Industries, Inc.. The 510(k) number is K901217.

When did TRIA-SONIC ULTRA SOUND TRANSMISSION GEL receive FDA 510(k) clearance?

TRIA-SONIC ULTRA SOUND TRANSMISSION GEL received FDA 510(k) clearance on 1990-06-22, under 510(k) number K901217.

Who is the listed applicant for TRIA-SONIC ULTRA SOUND TRANSMISSION GEL?

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

What is the FDA product code for TRIA-SONIC ULTRA SOUND TRANSMISSION GEL?

The FDA product code for TRIA-SONIC ULTRA SOUND TRANSMISSION GEL is JOT.

Related Clinical Trials

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Other records listing H & P Industries, 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.

K871169LUBRICATING JELLYK860961GAMMA RADIATION STERILIZED ALCOHOL PREP PADSK830393PROVIDONE-IODINE SWABSTICKSK830394PROVIDONE-IODINE PREP-PADS & TOWELETTES

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.K905545ULTRASOUND TRANSMISSION GELArbo Medical, Inc.K904418ULTRASOUND COUPLING GELGeno LaboratoriesK894490STERILE ULTRASOUND TRANSMISSION GELSwedish Trade Council USAK884503ULTRASONIC TRANSMISSION GELHerbert Stanley Co.K872519STERILIZED OMNI GELEcho Ultrasound

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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