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

SAGE 2200 STERILE SPECIMEN CONTAINER

K Number: K813408 · Decision Jan 25, 1982
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
91
Applicant Total
31
Review Days
49

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Basic Information

Device Name
SAGE 2200 STERILE SPECIMEN CONTAINER
K Number
K813408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sage Products, Inc.
Date Received
December 7, 1981
Decision Date
January 25, 1982
Product Code
FMT
Advisory Committee
General Hospital
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
FMT Warmer, Infant Radiant

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Other Clearances by Sage Products, Inc.

K Number Device Name
K972705 RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTIC
K980490 SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPS
K973911 2 GALLON ALTERNATE CARE SHARPS CONTAINER
K972279 SHARPS SHUTTLE
K970135 NITRILE GLOVES
K972302 POCKET COUNT OR SAFETCOUNT
K964168 PROCEDURE SPECIFIC KITS
K963986 STP SYSTEM PVA WITH ZINC
K964026 STP SYSTEM - SAF
K964027 STP SYSTEM-PVA WITH MERCURY
Search all 31 clearances from Sage Products, Inc. →