510(k) K770353

DISPOSABLE TEMPERATURE PROBE by Inhal-O-Tech Medical Plastic — Product Code KPD

K770353 is an FDA 510(k) premarket notification submitted by Inhal-O-Tech Medical Plastic for the device "DISPOSABLE TEMPERATURE PROBE". The FDA issued a decision of Substantially Equivalent on March 16, 1977. The device falls under product code KPD (Strip, Temperature, Forehead, Liquid Crystal), a Class II device regulated under 21 CFR 880.2200. Inhal-O-Tech Medical Plastic has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 16, 1977
Date Received
February 22, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Strip, Temperature, Forehead, Liquid Crystal
Device Class
Class II
Regulation Number
880.2200
Review Panel
HO
Submission Type