MICROLET FAMILY OF NEEDLE/DEPTH ELECT-

Electrode, Depth

PROGRESS MANKIND TECHNOLOGY

The following data is part of a premarket notification filed by Progress Mankind Technology with the FDA for Microlet Family Of Needle/depth Elect-.

Pre-market Notification Details

Device IDK802249
510k NumberK802249
Device Name:MICROLET FAMILY OF NEEDLE/DEPTH ELECT-
ClassificationElectrode, Depth
Applicant PROGRESS MANKIND TECHNOLOGY BOX 464 Hopkins,  MN  55343
ContactAlfred A Iversen
CorrespondentAlfred A Iversen
PROGRESS MANKIND TECHNOLOGY BOX 464 Hopkins,  MN  55343
Product CodeGZL  
CFR Regulation Number882.1330 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-09-16
Decision Date1980-11-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.