OPEN END SPRING GUIDE

Wire, Guide, Catheter

C.R. BARD, INC.

The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Open End Spring Guide.

Pre-market Notification Details

Device IDK832607
510k NumberK832607
Device Name:OPEN END SPRING GUIDE
ClassificationWire, Guide, Catheter
Applicant C.R. BARD, INC. 110 MARSHALL DRIVE Warrandale,  PA  15086
Product CodeDQX  
CFR Regulation Number870.1330 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-08-03
Decision Date1983-12-27

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20643169856664 K832607 000
20643169856657 K832607 000
20643169856640 K832607 000
20643169856633 K832607 000

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