LFT - 212

Monitor, Penile Tumescence

MEDICAL MONITORING SYSTEMS, INC.

The following data is part of a premarket notification filed by Medical Monitoring Systems, Inc. with the FDA for Lft - 212.

Pre-market Notification Details

Device IDK841879
510k NumberK841879
Device Name:LFT - 212
ClassificationMonitor, Penile Tumescence
Applicant MEDICAL MONITORING SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeLIL  
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-05-07
Decision Date1984-07-26

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