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

2 GALLON ALTERNATE CARE SHARPS CONTAINER

K Number: K973911 · Decision Oct 29, 1997
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
31
Review Days
15

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Basic Information

Device Name
2 GALLON ALTERNATE CARE SHARPS CONTAINER
K Number
K973911
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sage Products, Inc.
Date Received
October 14, 1997
Decision Date
October 29, 1997
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

Similar 510(k) Clearances

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

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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
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
K962168 MUCUS SPECIMEN TRAP
Search all 31 clearances from Sage Products, Inc. →