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

URESIL ABSCESS DRIANAGE AND IRRIGATION SET

K Number: K925117 · Decision Aug 11, 1993
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
45
Review Days
306

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Basic Information

Device Name
URESIL ABSCESS DRIANAGE AND IRRIGATION SET
K Number
K925117
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Uresil Corp.
Date Received
October 9, 1992
Decision Date
August 11, 1993
Product Code
GBX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBX Catheter, Irrigation

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K981344 URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATING
K980282 URESIL DILATOR WITH RADIOPAQUE MARKER
K980889 URESIL NEPHRO-URETERAL STENT
K972582 URESIL GUIDEWIRE
K972583 URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL BILIARY CATHETER, URESIL NEPHRO-URETERAL S
K953923 URESIL INTRODUCING NEEDLE
K945934 URESIL(R) GUIDEWIRE
K942688 NEPHRO-URETERAL STENT
Search all 45 clearances from Uresil Corp. →