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

MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

K Number: K911099 · Decision Jun 25, 1991
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
13
Applicant Total
39
Review Days
105

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE
K Number
K911099
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
March 12, 1991
Decision Date
June 25, 1991
Product Code
DWX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWX Stripper, Artery, Intraluminal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DWX), ordered by most recent decision date.

View all

Other Clearances by Pilling Co.

K Number Device Name
K934427 PILLING LAPAROSCOPIC INSTRUMENTATION
K925370 TRIANGULAR JAW MICROLARYNGEAL FORCEPS
K925198 KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR
K922971 NO-SCALPEL VASCETOMY INSTRUMENTS
K914015 CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP
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
Search all 39 clearances from Pilling Co. →