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

HEADLIGHTS W/ FILTER-OPTICO CABLES

K Number: K761142 · Decision Jan 5, 1977
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
44
Applicant Total
39
Review Days
40

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Basic Information

Device Name
HEADLIGHTS W/ FILTER-OPTICO CABLES
K Number
K761142
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
November 26, 1976
Decision Date
January 5, 1977
Product Code
FST
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
FST Light, Surgical, Fiberoptic

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K922971 NO-SCALPEL VASCETOMY INSTRUMENTS
K914015 CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP
K911099 MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE
K911100 MEHIGAN-PILLING PHLEBETOME TM
K904507 PILLING BRUSH VALVULOTOME
K884946 JEHLE CORONARY PERFUSION CATHETERS
K882930 LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX
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