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

POC ARTHROSCOPE AND ACCESSORIES

K Number: K945684 · Decision Jun 14, 1995
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
3
Review Days
205

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Basic Information

Device Name
POC ARTHROSCOPE AND ACCESSORIES
K Number
K945684
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precision Optics Corp.
Date Received
November 21, 1994
Decision Date
June 14, 1995
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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Other Clearances by Precision Optics Corp.

K Number Device Name
K053425 PRECISION OPTICS CORPORATION VIDEO OPHTHALMOSCOPE, MODEL 2500-VOS
K983123 POC ENT ENDOSCOPE - SINUSCOPE