510(k) K183067

Guardian Angel Rx GA2000 Digital Vital Sign Monitoring System by Taiwan Aulisa Medical Devices Technologies, Inc. — Product Code DQA

K183067 is an FDA 510(k) premarket notification submitted by Taiwan Aulisa Medical Devices Technologies, Inc. for the device "Guardian Angel Rx GA2000 Digital Vital Sign Monitoring System". The FDA issued a decision of Substantially Equivalent on March 1, 2019. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Taiwan Aulisa Medical Devices Technologies, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 1, 2019
Date Received
November 5, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Oximeter
Device Class
Class II
Regulation Number
870.2700
Review Panel
AN
Submission Type