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

RMI INTERNAL MAMMARY ARTERY CANNULA

K Number: K960098 · Decision Mar 26, 1996
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
24
Applicant Total
35
Review Days
75

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Basic Information

Device Name
RMI INTERNAL MAMMARY ARTERY CANNULA
K Number
K960098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Research Medical, Inc.
Date Received
January 11, 1996
Decision Date
March 26, 1996
Product Code
DQR
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
DQR Cannula, Catheter

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Other Clearances by Research Medical, Inc.

K Number Device Name
K970739 RMI HEMOCONCENTRATOR PREFERENCE PACK
K964833 RMI DUAL FLUID IRRIGATING SYRINGE
K961927 RMI HEMOCONCENTRACTOR TUBING SET
K951344 RMI HEMOCONCENTRATOR
K922083 RMI SURGICCAL SITE VISUALIZATION WAND
K920936 RMI EXTERNAL CORONARY ARTERY OCCLUDER
K915869 RMI NORMOCLUDER CORONARY ARTERY OCCLUDER
K920676 RMI SOFCLAMP
K910221 RMI VASCULAR TOURNIQUET KIT
K901231 RMI CARDIOPLEGIA DELIVERY KITS
Search all 35 clearances from Research Medical, Inc. →