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

AIR UTERINE DISPLACER-AUD 120

K Number: K833022 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
279
Registration Numbers
280
Same Product Code
7
Applicant Total
11
Review Days
38

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Basic Information

Device Name
AIR UTERINE DISPLACER-AUD 120
K Number
K833022
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6820
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Scientific Sales Intl., Inc.
Date Received
September 6, 1983
Decision Date
October 14, 1983
Product Code
CCX
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CCX Support, Patient Position

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