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

SURGITEK (R) UROFLOW SYSTEM

K Number: K883274 · Decision Feb 8, 1989
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
16
Applicant Total
28
Review Days
189

Basic Information

Device Name
SURGITEK (R) UROFLOW SYSTEM
K Number
K883274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1800
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
MEDICAL ENGINEERING CORP.
Date Received
August 3, 1988
Decision Date
February 8, 1989
Product Code
FFG
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
FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable

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Other Clearances by MEDICAL ENGINEERING CORP.

K Number Device Name
K934141 STAND ALONE CYSTOMETROGRAM
K905289 SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT
K903448 SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDER
K902773 SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SET
K884746 SURGITEK FLAT T-SPAN
K881736 SURGITEK CO2 DELIVERY SYSTEM
K880802 SURGITEK ARTICULATING URETEROSCOPE MODEL SU-11
K880801 SURGITEK FLEXIBLE URETEROSCOPE SU-7 & SU-9
K842748 SURGITEK RECONSTRUC-NIPPLE PROSTHESIS
K832043 SURGIKEK PENILE PROSTHESIS TAIL EXTEND
Search all 28 clearances from MEDICAL ENGINEERING CORP. →