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

MEDLINE STERISET STERILIZATION CONTAINER

K Number: K010825 · Decision May 8, 2001
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
11
Review Days
50

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Basic Information

Device Name
MEDLINE STERISET STERILIZATION CONTAINER
K Number
K010825
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medline
Date Received
March 19, 2001
Decision Date
May 8, 2001
Product Code
FRG
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
FRG Wrap, Sterilization

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K990463 MEDLINE EXCEL WHEELCHAIRS
K970282 MEDLINE CIRCUMCISION TRAY
K963504 MEDLINE OPEN END FINGER CONTROL MITT
K963452 MEDLINE ZIPPER SLEEVED VEST
K951736 LOCK-UP
K932033 LAPAROSCOPIC SURGERY INSTRUMENTS
K932060 MARTIN COLD LIGHT FOUNTAIN
K915502 MEDLINE, GORE-TEX BARRIER, SURGICAL GOWNS & DRAPES
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