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

REDDICK RETRACTOR

K Number: K915175 · Decision Apr 29, 1992
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
16
Review Days
166

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Basic Information

Device Name
REDDICK RETRACTOR
K Number
K915175
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 15, 1991
Decision Date
April 29, 1992
Product Code
GAD
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
GAD Retractor

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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
K914880 DUAL BALLOON EMBOLECTOMY CATHETER
K913602 IDEAS' PORT
K914913 GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST
K912540 CONTOUR-PORT
K911601 REDDICK TROCAR AND CANNULA
Search all 16 clearances from Ideal Medical, Inc. →