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FDA 510(k)

RFG-DGP DISPOSABLE GROUNDING PADS

K-Number: K923647 · 1992-11-09

ApplicantRadionics, Inc.
Decision Date1992-11-09
Product CodeJOT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RFG-DGP DISPOSABLE GROUNDING PADS is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K923647. 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 RFG-DGP DISPOSABLE GROUNDING PADS?

RFG-DGP DISPOSABLE GROUNDING PADS is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Radionics, Inc.. The 510(k) number is K923647.

When did RFG-DGP DISPOSABLE GROUNDING PADS receive FDA 510(k) clearance?

RFG-DGP DISPOSABLE GROUNDING PADS received FDA 510(k) clearance on 1992-11-09, under 510(k) number K923647.

Who is the listed applicant for RFG-DGP DISPOSABLE GROUNDING PADS?

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

What is the FDA product code for RFG-DGP DISPOSABLE GROUNDING PADS?

The FDA product code for RFG-DGP DISPOSABLE GROUNDING PADS is JOT.

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Other records listing Radionics, 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.

K030697RADIONICS SINGLE USE GROUND PAD (DGP-HP)K002773NEUROMAP WITH NEURO 100K001741RADIONICS RF DISC CATHETER ELECTRODE SYSTEMK992226XDS EXTERNAL CSF DRAINAGE AND MONITORING SYSTEMK001950OPTICAL TRACKING SYSTEM (OTS)K001700XPLAN 2.1

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Related Devices (Code: JOT)

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K905545ULTRASOUND TRANSMISSION GELArbo Medical, 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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