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

FRAZIER SUCTION INSTRUMENT-DISPOS

K Number: K832636 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
39
Review Days
71

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
FRAZIER SUCTION INSTRUMENT-DISPOS
K Number
K832636
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
August 4, 1983
Decision Date
October 14, 1983
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEA), 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
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
Search all 39 clearances from Pilling Co. →