PHOTOMETER LP 6

Colorimeter, Photometer, Spectrophotometer For Clinical Use

DR. BRUNO LANGE GMBH

The following data is part of a premarket notification filed by Dr. Bruno Lange Gmbh with the FDA for Photometer Lp 6.

Pre-market Notification Details

Device IDK801562
510k NumberK801562
Device Name:PHOTOMETER LP 6
ClassificationColorimeter, Photometer, Spectrophotometer For Clinical Use
Applicant DR. BRUNO LANGE GMBH 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJJQ  
CFR Regulation Number862.2300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-07-08
Decision Date1980-08-20

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