27-210 PLASTER KNIFE (REINER)

Knife, Surgical

ARTIBERIA

The following data is part of a premarket notification filed by Artiberia with the FDA for 27-210 Plaster Knife (reiner).

Pre-market Notification Details

Device IDK851784
510k NumberK851784
Device Name:27-210 PLASTER KNIFE (REINER)
ClassificationKnife, Surgical
Applicant ARTIBERIA 4518 LOS RANCHITOS San Antonio,  TX  78233
ContactGil M Sanchez
CorrespondentGil M Sanchez
ARTIBERIA 4518 LOS RANCHITOS San Antonio,  TX  78233
Product CodeEMF  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-04-25
Decision Date1985-06-20

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