510(k) K002395

MODEL 30 CLASSIC PNEUMATONOMETER by Xomed, Inc. — Product Code HKX

K002395 is an FDA 510(k) premarket notification submitted by Xomed, Inc. for the device "MODEL 30 CLASSIC PNEUMATONOMETER". The FDA issued a decision of Substantially Equivalent on December 11, 2000. The device falls under product code HKX (Tonometer, Ac-Powered), a Class II device regulated under 21 CFR 886.1930. Xomed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 11, 2000
Date Received
August 7, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tonometer, Ac-Powered
Device Class
Class II
Regulation Number
886.1930
Review Panel
OP
Submission Type