Abbott Medical Grounding Pad, Model RF-DGP-IS

Generator, Lesion, Radiofrequency

Abbott Medical

The following data is part of a premarket notification filed by Abbott Medical with the FDA for Abbott Medical Grounding Pad, Model Rf-dgp-is.

Pre-market Notification Details

Device IDK203293
510k NumberK203293
Device Name:Abbott Medical Grounding Pad, Model RF-DGP-IS
ClassificationGenerator, Lesion, Radiofrequency
Applicant Abbott Medical 5050 Nathan Lane Plymouth,  MN  55442
ContactJordan Hanson
CorrespondentJordan Hanson
Abbott Medical 5050 Nathan Lane Plymouth,  MN  55442
Product CodeGXD  
CFR Regulation Number882.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-11-09
Decision Date2022-01-21

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
15415067034516 K203293 000
05415067049650 K203293 000

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