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

SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SET

K Number: K902773 · Decision Jul 16, 1990
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
103
Applicant Total
28
Review Days
21

Basic Information

Device Name
SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SET
K Number
K902773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
MEDICAL ENGINEERING CORP.
Date Received
June 25, 1990
Decision Date
July 16, 1990
Product Code
FGB
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
FGB Ureteroscope And Accessories, Flexible/Rigid

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Other Clearances by MEDICAL ENGINEERING CORP.

K Number Device Name
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K903448 SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDER
K884746 SURGITEK FLAT T-SPAN
K883274 SURGITEK (R) UROFLOW SYSTEM
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
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