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

MODEL DMC-75 MINI-CATHETER SET

K Number: K874307 · Decision Jan 29, 1988
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
68
Review Days
101

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Basic Information

Device Name
MODEL DMC-75 MINI-CATHETER SET
K Number
K874307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Life-Tech Intl., Inc.
Date Received
October 20, 1987
Decision Date
January 29, 1988
Product Code
FPA
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
FPA Set, Administration, Intravascular

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Other Clearances by Life-Tech Intl., Inc.

K Number Device Name
K001129 PROLONG, MODELS PL50, PL100, PL150
K955031 MAXISTIM
K954505 EZ STIM
K954315 PVC ABDOMINAL/RECTAL PRESSURE CATHETER
K954341 URODYNAMICS TUBING AND INFUSION SETS
K953451 UROPUMP TUBE & DAMPING CHAMGER
K953353 UROVISION JANUS
K946108 EAR-A-GATOR
K913601 MICROPHOR
K940203 TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
Search all 68 clearances from Life-Tech Intl., Inc. →