Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by AMPLIFE CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K043550
12/23/2004
AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100
AMPLIFE CORPORATION
K050413
02/18/2005
AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600
AMPLIFE CORPORATION
K042575
09/22/2004
AMPLIFE DIGITAL CLINICAL THERMOMETER
AMPLIFE CORPORATION
K042906
10/21/2004
AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101
AMPLIFE CORPORATION
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact