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

MINI-MICRO ARTHROSCOPIC SCAPEL

K Number: K820777 · Decision May 12, 1982
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
60
Review Days
50

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Basic Information

Device Name
MINI-MICRO ARTHROSCOPIC SCAPEL
K Number
K820777
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
The Anspach Effort, Inc.
Date Received
March 23, 1982
Decision Date
May 12, 1982
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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