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

PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER

K Number: K952414 · Decision Jun 23, 1995
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
12
Review Days
31

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Basic Information

Device Name
PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER
K Number
K952414
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acacia Laboratories, Inc.
Date Received
May 23, 1995
Decision Date
June 23, 1995
Product Code
KNY
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
KNY Accessories, Catheter, G-U

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Other Clearances by Acacia Laboratories, Inc.

K Number Device Name
K952419 STERIGAUZE GEL DRESSING
K952420 STERIGAUZE WET DRESSING
K951861 STERICARE WOUND CARE GEL
K951914 HYDRACARE ABSORBENT WOUND DRESSING
K950344 HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER
K913408 STERILE PLASTIC DRAPE
K901761 STERILE SUCTION TUBING SET
K892856 NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
K892804 NEWCHILL(TM) CARDIAC INSULATOR
K884055 SURGI-TAG(TM) STERILE LABEL SETS
Search all 12 clearances from Acacia Laboratories, Inc. →