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

GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST

K Number: K914913 · Decision Dec 31, 1991
Classifications
1
FEI Numbers
270
Registration Numbers
270
Same Product Code
31
Applicant Total
16
Review Days
60

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
GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST
K Number
K914913
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ideal Medical, Inc.
Date Received
November 1, 1991
Decision Date
December 31, 1991
Product Code
GDJ
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
GDJ Clamp, Surgical, General & Plastic Surgery

Similar 510(k) Clearances

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

View all

Other Clearances by Ideal Medical, Inc.

K Number Device Name
K944067 PEANUT WAND, MODIFICATION
K931115 HATCHER STONE-EMBOLIS EXTRACTOR
K926335 IDEAS PEANUT WAND
K922161 GRICE SOFT TISSUE BIOPSY KIT
K921922 GRICE LAPAROSCOPIC SUTURING NEEDLE
K915175 REDDICK RETRACTOR
K914880 DUAL BALLOON EMBOLECTOMY CATHETER
K913602 IDEAS' PORT
K912540 CONTOUR-PORT
K911601 REDDICK TROCAR AND CANNULA
Search all 16 clearances from Ideal Medical, Inc. →