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

RICHARDS INTRA-ARTICULAR SHAVER BLADES

K Number: K830153 · Decision Feb 28, 1983
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
40
Applicant Total
48
Review Days
41

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
RICHARDS INTRA-ARTICULAR SHAVER BLADES
K Number
K830153
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Richard'S Medical Equip., Inc.
Date Received
January 18, 1983
Decision Date
February 28, 1983
Product Code
GEY
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
GEY Motor, Surgical Instrument, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Richard'S Medical Equip., Inc.

K Number Device Name
K830793 PATIENT GUIDED ELBOW & SHOULDER EXERC
K823837 RMC TOTAL KNEE SYSTEM
K823726 SPECTRON CONVERSION ENDOPROSTHESIS CUP
K823724 SPECTRON NECK REPLACEMENT PROSTHESIS
K823723 SPECTRON PROXIMAL FEMORAL PROSTHESIS
K823722 SPECTRON LONG, STRAIGHT FEMORAL PROSTHES
K823727 SPECTRON PRIMARY STEM FEMORAL PROSTHES
K830154 COLLES FRACTURE FRAME
K823725 SPECTRON PROTRUSIO CUP
K823728 SPECTRON POLYETHYLENE ACCTUBULAR COMPON
Search all 48 clearances from Richard'S Medical Equip., Inc. →