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

MED-A-CALL ASSIST DEVICE

K Number: K890596 · Decision Mar 14, 1989
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
2
Review Days
46

Basic Information

Device Name
MED-A-CALL ASSIST DEVICE
K Number
K890596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3725
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
SILENT CALL CORP.
Date Received
January 27, 1989
Decision Date
March 14, 1989
Product Code
IQA
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
IQA System, Environmental Control, Powered

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Other Clearances by SILENT CALL CORP.

K Number Device Name
K890445 PERSONAL ALERT ASSIST DEVICE