510(k) K821966

MODULUS VERNI-TROL ANESTHETIC VAPORIZER by Ohio Medical Products — Product Code CAD

K821966 is an FDA 510(k) premarket notification submitted by Ohio Medical Products for the device "MODULUS VERNI-TROL ANESTHETIC VAPORIZER". The FDA issued a decision of Substantially Equivalent on July 16, 1982. The device falls under product code CAD (Vaporizer, Anesthesia, Non-Heated), a Class II device regulated under 21 CFR 868.5880. Ohio Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 1982
Date Received
July 2, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Vaporizer, Anesthesia, Non-Heated
Device Class
Class II
Regulation Number
868.5880
Review Panel
AN
Submission Type