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

SHUTT PRECISION PROBES

K Number: K840558 · Decision Apr 25, 1984
Classifications
1
FEI Numbers
373
Registration Numbers
373
Same Product Code
14
Applicant Total
83
Review Days
77

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Basic Information

Device Name
SHUTT PRECISION PROBES
K Number
K840558
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
February 8, 1984
Decision Date
April 25, 1984
Product Code
HXB
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
HXB Probe

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K892376 INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)
K891109 PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
K881954 CONCEPT POWER SYSTEM
K884255 CONCEPT CCT-5200, THERMAL THERAPY SYSTEM
K882121 C-FLO SUCTION TUBE
K880414 TENDON HARVESTER
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