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

LIFEBED NETWORK PATIENT VIGILANCE SYSTEM

K Number: K083534 · Decision Apr 13, 2009
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
5
Review Days
136

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Basic Information

Device Name
LIFEBED NETWORK PATIENT VIGILANCE SYSTEM
K Number
K083534
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hoana Medical, Inc.
Date Received
November 28, 2008
Decision Date
April 13, 2009
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DRT), ordered by most recent decision date.

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Other Clearances by Hoana Medical, Inc.

K Number Device Name
K100745 LIFEBED NETWORK PATIENT VIGILANCE SYSTEM
K092037 LIFEGURNEY NETWORK PATIENT VIGILANCE SYSTEM
K082366 LIFEBED PATIENT VIGILANCE SYSTEM
K052446 LG1 INTELLIGENT MEDICAL VIGILANCE SYSTEM