510(k) K940333

EYE PAD by Certified Safety Mfg., Inc. — Product Code HMP

K940333 is an FDA 510(k) premarket notification submitted by Certified Safety Mfg., Inc. for the device "EYE PAD". The FDA issued a decision of Substantially Equivalent on March 7, 1994. The device falls under product code HMP (Pad, Eye), a Class I device regulated under 21 CFR 878.4440. Certified Safety Mfg., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 1994
Date Received
January 25, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pad, Eye
Device Class
Class I
Regulation Number
878.4440
Review Panel
SU
Submission Type