VISITEC NEEDLE RANGE (ANESTHESIOLOGY)

Needle, Conduction, Anesthetic (w/wo Introducer)

VISITEC CO.

The following data is part of a premarket notification filed by Visitec Co. with the FDA for Visitec Needle Range (anesthesiology).

Pre-market Notification Details

Device IDK811963
510k NumberK811963
Device Name:VISITEC NEEDLE RANGE (ANESTHESIOLOGY)
ClassificationNeedle, Conduction, Anesthetic (w/wo Introducer)
Applicant VISITEC CO. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeBSP  
CFR Regulation Number868.5150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-07-10
Decision Date1981-07-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.