EFFRON PAROTID RETRACTOR

Retractor

AMERICAN V. MUELLER

The following data is part of a premarket notification filed by American V. Mueller with the FDA for Effron Parotid Retractor.

Pre-market Notification Details

Device IDK801759
510k NumberK801759
Device Name:EFFRON PAROTID RETRACTOR
ClassificationRetractor
Applicant AMERICAN V. MUELLER 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGAD  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-07-28
Decision Date1980-08-20

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