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

SIEMENS NEUROTON 826 AND 827

K Number: K875238 · Decision Mar 10, 1988
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
26
Review Days
79

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Basic Information

Device Name
SIEMENS NEUROTON 826 AND 827
K Number
K875238
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Elmed, Inc.
Date Received
December 22, 1987
Decision Date
March 10, 1988
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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Other Clearances by Elmed, Inc.

K Number Device Name
K010465 DENSTAT
K974793 ELMED ESU 120 M/M DIGITAL
K953271 ELMED RF-ALERT
K952110 ELMED THERMO-FLUX
K926517 ELMED LBC 50-P
K932938 ELMED ESU 300 M/M AND DIGITAL
K921770 ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M
K915731 ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL
K905417 ELMED PNEUMOMAT DIGITAL
K881431 SIEMENS STEREODYNATOR 828
Search all 26 clearances from Elmed, Inc. →