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

CADIO-RESPIRATORY MONITOR #CR-2

K Number: K823312 · Decision Nov 30, 1982
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
23
Review Days
25

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Basic Information

Device Name
CADIO-RESPIRATORY MONITOR #CR-2
K Number
K823312
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Electromed Intl., Ltd.
Date Received
November 5, 1982
Decision Date
November 30, 1982
Product Code
DRT
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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Other Clearances by Electromed Intl., Ltd.

K Number Device Name
K003688 VIEW READING STATION
K000474 VIEW NT
K990759 VIEW COM
K974255 CD-R STATION AND VRS-2000
K971176 VIEW ARCHIVING STATION
K950694 COMPACT-X
K880050 EDEC 60R
K875341 EDEC 60 R/F
K875342 EDEC 90C
K871145 EDEC 50C CONSTANT POTENTIAL X-RAY GENERATOR
Search all 23 clearances from Electromed Intl., Ltd. →