CENTAURI/PEGASUS

Powered Laser Surgical Instrument

PFIZER LASER SYSTEMS

The following data is part of a premarket notification filed by Pfizer Laser Systems with the FDA for Centauri/pegasus.

Pre-market Notification Details

Device IDK905737
510k NumberK905737
Device Name:CENTAURI/PEGASUS
ClassificationPowered Laser Surgical Instrument
Applicant PFIZER LASER SYSTEMS 3 MORGAN Irvine,  CA  92718
ContactColette Cozean
CorrespondentColette Cozean
PFIZER LASER SYSTEMS 3 MORGAN Irvine,  CA  92718
Product CodeGEX  
CFR Regulation Number878.4810 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-12-24
Decision Date1991-06-17

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