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

MODEL #510/515 GENERAL TRANSPORT STRETCHER

K Number: K895016 · Decision Sep 11, 1989
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
34
Applicant Total
31
Review Days
34

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Basic Information

Device Name
MODEL #510/515 GENERAL TRANSPORT STRETCHER
K Number
K895016
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3750
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Midmark Corp.
Date Received
August 8, 1989
Decision Date
September 11, 1989
Product Code
INW
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
INW Table, Mechanical

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