VESSEL LOOPS

Scalpel, One-piece

APPLIED MEDICAL TECHNOLOGIES

The following data is part of a premarket notification filed by Applied Medical Technologies with the FDA for Vessel Loops.

Pre-market Notification Details

Device IDK895682
510k NumberK895682
Device Name:VESSEL LOOPS
ClassificationScalpel, One-piece
Applicant APPLIED MEDICAL TECHNOLOGIES 6100 WEST CREEK RD. SUITE 25 Independence,  OH  44131
ContactDean Secrest
CorrespondentDean Secrest
APPLIED MEDICAL TECHNOLOGIES 6100 WEST CREEK RD. SUITE 25 Independence,  OH  44131
Product CodeGDX  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-09-21
Decision Date1989-10-24

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