FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

THE MEDCOMP .010 VASCULAR GUIDEWIRES

K Number: K081775 · Decision Mar 25, 2009
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
40
Review Days
275

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Basic Information

Device Name
THE MEDCOMP .010 VASCULAR GUIDEWIRES
K Number
K081775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medcomp
Date Received
June 23, 2008
Decision Date
March 25, 2009
Product Code
DQX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQX Wire, Guide, Catheter

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Other Clearances by Medcomp

K Number Device Name
K130889 SPLIT CATH RG
K123292 T3
K102966 2.6F X 20CM VASCU-PICC, 2.6F X 50CM VASCU-PICC
K091954 MICRO-STICK SET
K092347 PRO-PICC CT
K091953 PRO-PICC
K090394 VALVED TEARWAY INTRODUCER
K091586 VASCU-PICC AND MIDLINE CATHETERS, SINGLE, DOUBLE AND TRIPLE LUMEN
K091466 1.9F X 20CM VASCU-PICC, 1.9F X 50CM VASCU-PICC, MODEL VPI.9S20, VPI.9S50
K081904 PRO-PICC (BASIC TRAY, LONG WIRE TRAY, BASIC NURSING TRAY, FULL NURSING TRAY)
Search all 40 clearances from Medcomp →