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

NO-SCALPEL VASCETOMY INSTRUMENTS

K Number: K922971 · Decision Sep 23, 1992
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
43
Applicant Total
39
Review Days
96

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Basic Information

Device Name
NO-SCALPEL VASCETOMY INSTRUMENTS
K Number
K922971
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pilling Co.
Date Received
June 19, 1992
Decision Date
September 23, 1992
Product Code
KOA
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
KOA Surgical Instruments, G-U, Manual (And Accessories)

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Other Clearances by Pilling Co.

K Number Device Name
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K925198 KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR
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
K874242 JEHLE CORONARY PERFUSION CATHETERS
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