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

SURGITEK MEDI-LOOPS

K Number: K803156 · Decision Jan 15, 1981
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
28
Review Days
34

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Basic Information

Device Name
SURGITEK MEDI-LOOPS
K Number
K803156
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Medical Engineering Corp.
Date Received
December 12, 1980
Decision Date
January 15, 1981
Product Code
KDC
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
KDC Instrument, Surgical, 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
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
Search all 28 clearances from Medical Engineering Corp. →