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

PEDIATRIC URINE COLLECTOR

K Number: K823411 · Decision Dec 28, 1982
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
31
Review Days
43

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Basic Information

Device Name
PEDIATRIC URINE COLLECTOR
K Number
K823411
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Sage Products, Inc.
Date Received
November 15, 1982
Decision Date
December 28, 1982
Product Code
KNX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNX Collector, Urine, (And Accessories) For Indwelling Catheter

Similar 510(k) Clearances

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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
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