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

RICHARD ARTHROSCOPE

K Number: K843604 · Decision Oct 22, 1984
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
71
Review Days
39

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Basic Information

Device Name
RICHARD ARTHROSCOPE
K Number
K843604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Richards Medical Co., Inc.
Date Received
September 13, 1984
Decision Date
October 22, 1984
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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K Number Device Name
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K895241 INTRAMEDULLARY HIP SCREW
K884824 TRICON-M TOTAL KNEE SYSTEM
K896204 ZIRCONIA CERAMIC HEAD ADD'L SIZES
K895242 PAPPAS TRI-FLANGE VENTILATION TUBE
K893377 RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS
K885069 ZIRCONIA CERAMIC HEAD (YITRIA STABILIZED)
K892366 POROUS GENESIS STEMMED TIBIAL COMPONENT
Search all 71 clearances from Richards Medical Co., Inc. →