MICROTEK PROBE DRAPE

Drape, Surgical

MICROBIO-MEDICS, INC.

The following data is part of a premarket notification filed by Microbio-medics, Inc. with the FDA for Microtek Probe Drape.

Pre-market Notification Details

Device IDK882724
510k NumberK882724
Device Name:MICROTEK PROBE DRAPE
ClassificationDrape, Surgical
Applicant MICROBIO-MEDICS, INC. POST OFFICE BOX 2487 Columbus,  MS  39704
ContactKeith Mcgee
CorrespondentKeith Mcgee
MICROBIO-MEDICS, INC. POST OFFICE BOX 2487 Columbus,  MS  39704
Product CodeKKX  
CFR Regulation Number878.4370 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-07-01
Decision Date1988-08-03

NIH GUDID Devices

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