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

SURGITEK FOERSTER FACE LIFT DRAIN

K Number: K800331 · Decision Mar 5, 1980
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
28
Review Days
21

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Basic Information

Device Name
SURGITEK FOERSTER FACE LIFT DRAIN
K Number
K800331
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Medical Engineering Corp.
Date Received
February 13, 1980
Decision Date
March 5, 1980
Product Code
GCY
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
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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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
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