KARL STORZ INTUBATION FIBERSCOPE

Bronchoscope (flexible Or Rigid)

KARL STORZ ENDOSCOPY-AMERICA, INC.

The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Karl Storz Intubation Fiberscope.

Pre-market Notification Details

Device IDK961178
510k NumberK961178
Device Name:KARL STORZ INTUBATION FIBERSCOPE
ClassificationBronchoscope (flexible Or Rigid)
Applicant KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City,  CA  90230 -7600
ContactRenate A Maclaren
CorrespondentRenate A Maclaren
KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City,  CA  90230 -7600
Product CodeEOQ  
CFR Regulation Number874.4680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-03-26
Decision Date1996-05-14
Summary:summary

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