510(k) K990082

EPIC SPO2 FINGER SENSOR, MODEL E403-09, E412-09 AND EPIC OXIMETER CABLE, MODEL E710-09 by Epic Medical Equipment Services, Inc. — Product Code DQA

K990082 is an FDA 510(k) premarket notification submitted by Epic Medical Equipment Services, Inc. for the device "EPIC SPO2 FINGER SENSOR, MODEL E403-09, E412-09 AND EPIC OXIMETER CABLE, MODEL E710-09". The FDA issued a decision of Substantially Equivalent on April 9, 1999. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Epic Medical Equipment Services, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 9, 1999
Date Received
January 11, 1999
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