FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

IV START KIT

K Number: K914475 · Decision Mar 18, 1992
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
29
Applicant Total
26
Review Days
162

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Basic Information

Device Name
IV START KIT
K Number
K914475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Cypress Medical Products, Ltd.
Date Received
October 8, 1991
Decision Date
March 18, 1992
Product Code
LRS
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRS I.V. Start Kit

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Other Clearances by Cypress Medical Products, Ltd.

K Number Device Name
K021676 CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL
K012282 STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
K972899 CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER
K972849 ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
K972883 ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
K952367 CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE
K950254 CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE
K950092 CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY
K950109 CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY/WITH OUT CATHETER
K945082 CYPRESS MEDICAL PRODUCTS STETHOSCOPE
Search all 26 clearances from Cypress Medical Products, Ltd. →