FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RMI DUAL FLUID IRRIGATING SYRINGE

K Number: K964833 · Decision Feb 19, 1997
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
40
Applicant Total
35
Review Days
79

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Basic Information

Device Name
RMI DUAL FLUID IRRIGATING SYRINGE
K Number
K964833
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6960
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Research Medical, Inc.
Date Received
December 2, 1996
Decision Date
February 19, 1997
Product Code
KYZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KYZ Syringe, Irrigating (Non Dental)

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Other Clearances by Research Medical, Inc.

K Number Device Name
K970739 RMI HEMOCONCENTRATOR PREFERENCE PACK
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
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. →