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

MODIFIED EXTERNAL PAD

K Number: K891000 · Decision May 19, 1989
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
32
Review Days
81

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Basic Information

Device Name
MODIFIED EXTERNAL PAD
K Number
K891000
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Instromedix, Inc.
Date Received
February 27, 1989
Decision Date
May 19, 1989
Product Code
DWS
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
DWS Instruments, Surgical, Cardiovascular

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K951096 LIFESIGNS RECEIVING CENER 2000 TRANSTELEPHONIC RECEIVER
K945476 HEARTHWATCH III(TM)
K950003 CARDIOMAGIC(R) SOFTWARE ENHANCEMENTS
K944362 HEARTCARD CARDIAC EVENT MONITOR
K943931 CARRYALL ENHANCEMENTS
K935586 PRINCE
K925639 CARDIOMAGIC SOFTWARE
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