510(k) K920824

Device
Roadrunner Rltf Guide Wire
Applicant
COOK, INC.
510(k) number
K920824
Product code
DQX
Decision
Substantially Equivalent (SESE)
Decision date
1992-10-16
Date received
1992-02-24
Regulation
870.1330
Classification name
Wire, Guide, Catheter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
APRIL LAVENDER
Address
925 S. Curry Pike P.O. Box 489 Bloomington IN US 47402 47402

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Other 510(k) Records For Product Code DQX

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