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

MNI 400 INJECTION CAPS

K Number: K852162 · Decision Jun 12, 1985
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
64
Applicant Total
11
Review Days
23

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Basic Information

Device Name
MNI 400 INJECTION CAPS
K Number
K852162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Med-West, Inc.
Date Received
May 20, 1985
Decision Date
June 12, 1985
Product Code
LFJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
LFJ Catheter, Subclavian

Similar 510(k) Clearances

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Other Clearances by Med-West, Inc.

K Number Device Name
K880877 CONTRAST INJECTION DEVICE
K880398 POWER TOILET ELEVATOR
K874470 MWI 400 WOUND DRESSING
K872724 SHEATH/DILATORS
K854612 ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7
K842342 MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN
K832124 CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI
K831828 TEFLON FEMORAL CATHETER MWI 100,10 &
K831401 SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS
K831440 SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260
Search all 11 clearances from Med-West, Inc. →