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

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE

K Number: K915393 · Decision Dec 17, 1991
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
17
Applicant Total
22
Review Days
18

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Basic Information

Device Name
MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE
K Number
K915393
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mdt Corp., Inc.
Date Received
November 29, 1991
Decision Date
December 17, 1991
Product Code
GDC
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
GDC Table, Operating-Room, Electrical

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K924380 MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
K926081 DENTAL LIGHT
K924955 MDT/HARVEY MC-8 AND MC-10
K932094 BOVIE ULTRASONIC SURGICAL ASPIRATOR
K931169 MDT DENTAL CHAIR
K920930 MDT/CASTLE 10/90 DUAL LOAD STATION
K922212 MDT CASTLE BIOSIGN TEST PACK
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