510(k) K940333
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