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

PLASTIC TUBING CONNECTOR

K Number: K874360 · Decision Nov 17, 1987
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
63
Applicant Total
6
Review Days
25

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Basic Information

Device Name
PLASTIC TUBING CONNECTOR
K Number
K874360
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
American Medical Technology, Inc.
Date Received
October 23, 1987
Decision Date
November 17, 1987
Product Code
FPK
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
FPK Tubing, Fluid Delivery

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Other Clearances by American Medical Technology, Inc.

K Number Device Name
K963808 CHOICE POWERED WHEELCHAIR
K905745 AMETEC MASY MODULAR ANGIOSCOPE SYSTEM
K874567 RESUSCITATOR
K874430 NEEDLE CONTAINER
K873313 SURGICAL DRAPE