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FDA 510(k)

RADIONICS SINGLE USE GROUND PAD (DGP-HP)

K-Number: K030697 · 2003-04-04

ApplicantRadionics, Inc.
Decision Date2003-04-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RADIONICS SINGLE USE GROUND PAD (DGP-HP) is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 2003-04-04 under 510(k) number K030697. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIONICS SINGLE USE GROUND PAD (DGP-HP)?

RADIONICS SINGLE USE GROUND PAD (DGP-HP) is a medical device that received FDA 510(k) clearance on 2003-04-04. The listed applicant is Radionics, Inc.. The 510(k) number is K030697.

When did RADIONICS SINGLE USE GROUND PAD (DGP-HP) receive FDA 510(k) clearance?

RADIONICS SINGLE USE GROUND PAD (DGP-HP) received FDA 510(k) clearance on 2003-04-04, under 510(k) number K030697.

Who is the listed applicant for RADIONICS SINGLE USE GROUND PAD (DGP-HP)?

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 RADIONICS SINGLE USE GROUND PAD (DGP-HP)?

The FDA product code for RADIONICS SINGLE USE GROUND PAD (DGP-HP) is GEI.

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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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