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

CENTURION STOPCOCK 3 WAY

K Number: K810375 · Decision Feb 26, 1981
Classifications
1
FEI Numbers
93
Registration Numbers
93
Same Product Code
88
Applicant Total
16
Review Days
14

Basic Information

Device Name
CENTURION STOPCOCK 3 WAY
K Number
K810375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
TRI-STATE HOSPITAL SUPPLY CORP.
Date Received
February 12, 1981
Decision Date
February 26, 1981
Product Code
FMG
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
FMG Stopcock, I.V. Set

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FMG), ordered by most recent decision date.

View all

Other Clearances by TRI-STATE HOSPITAL SUPPLY CORP.

K Number Device Name
K080448 CENTURION PROTECTIVE RESTRAINT, SCR SERIES
K080524 CENTURION SORBAVIEW OTC
K942353 CENTURION UMBILICAL CATHETER
K945977 CENTURION(R) SITE GUARD(R) TRANSPARENT DRESSING/TRANSPAENT FILM DRESSING
K931748 CENTLURION DISP STERI DENTAL/HYGIENE PACK/TRAYS
K935491 CENTURION MOGEN CLAMP/CIRCUMCISION (STER/NON STER)
K923812 CENTURION DISPOSABLE INSTRUMENTS
K910906 CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS
K897100 CENTURION VAGINAL SPECULUM
K896320 CENTURION KLEEN-NEEDLE SYSTEM
Search all 16 clearances from TRI-STATE HOSPITAL SUPPLY CORP. →