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FDA 510(k)

ULTRASONIC TRANSMISSION GEL

K-Number: K884503 · 1989-02-13

ApplicantHerbert Stanley Co.
Decision Date1989-02-13
Product CodeJOT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC TRANSMISSION GEL is the device name listed in this FDA 510(k) record. The listed applicant is Herbert Stanley Co.. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K884503. 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 ULTRASONIC TRANSMISSION GEL?

ULTRASONIC TRANSMISSION GEL is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Herbert Stanley Co.. The 510(k) number is K884503.

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

ULTRASONIC TRANSMISSION GEL received FDA 510(k) clearance on 1989-02-13, under 510(k) number K884503.

Who is the listed applicant for ULTRASONIC TRANSMISSION GEL?

The FDA 510(k) record lists Herbert Stanley Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASONIC TRANSMISSION GEL?

The FDA product code for ULTRASONIC TRANSMISSION GEL is JOT.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Herbert Stanley Co. 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.

K884504ELECTRODE GEL

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 LaboratoriesK901217TRIA-SONIC ULTRA SOUND TRANSMISSION GELH & P Industries, Inc.K894490STERILE ULTRASOUND TRANSMISSION GELSwedish Trade Council USAK872519STERILIZED 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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