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

RMI NORMOCLUDER CORONARY ARTERY OCCLUDER

K Number: K915869 · Decision Dec 8, 1992
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
89
Applicant Total
35
Review Days
343

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Basic Information

Device Name
RMI NORMOCLUDER CORONARY ARTERY OCCLUDER
K Number
K915869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Research Medical, Inc.
Date Received
December 31, 1991
Decision Date
December 8, 1992
Product Code
MJN
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
MJN Catheter, Intravascular Occluding, Temporary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MJN), ordered by most recent decision date.

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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
K960098 RMI INTERNAL MAMMARY ARTERY CANNULA
K951344 RMI HEMOCONCENTRATOR
K922083 RMI SURGICCAL SITE VISUALIZATION WAND
K920936 RMI EXTERNAL CORONARY ARTERY OCCLUDER
K920676 RMI SOFCLAMP
K910221 RMI VASCULAR TOURNIQUET KIT
K901231 RMI CARDIOPLEGIA DELIVERY KITS
Search all 35 clearances from Research Medical, Inc. →