510(k) K093306

SINGLE-PATIENT USE DISPOSABLE SENSOR by Nonin Medical, Inc. — Product Code DQA

K093306 is an FDA 510(k) premarket notification submitted by Nonin Medical, Inc. for the device "SINGLE-PATIENT USE DISPOSABLE SENSOR". The FDA issued a decision of Substantially Equivalent on March 4, 2010. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Nonin Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 2010
Date Received
October 22, 2009
Clearance Type
Special
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