510(k) K844253

NOVAMETRIX 811 TRANSCO2M PORTABLE TRANSCUTANEOUS 2 by Novametrix Medical Systems, Inc. — Product Code KLK

K844253 is an FDA 510(k) premarket notification submitted by Novametrix Medical Systems, Inc. for the device "NOVAMETRIX 811 TRANSCO2M PORTABLE TRANSCUTANEOUS 2". The FDA issued a decision of Substantially Equivalent on January 10, 1985. The device falls under product code KLK (Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia), a Class II device regulated under 21 CFR 868.2500. Novametrix Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 10, 1985
Date Received
November 2, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
Device Class
Class II
Regulation Number
868.2500
Review Panel
AN
Submission Type