FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NITRILE GLOVES

K Number: K970135 · Decision Aug 25, 1997
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
78
Applicant Total
31
Review Days
222

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Basic Information

Device Name
NITRILE GLOVES
K Number
K970135
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sage Products, Inc.
Date Received
January 15, 1997
Decision Date
August 25, 1997
Product Code
LZC
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
LZC Medical Glove, Specialty

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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
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. →