510(k) K030300
K030300 is an FDA 510(k) premarket notification submitted by Lacrimedics, Inc. for the device "OPAQUE HERRICK LACRIMAL PLUG". The FDA issued a decision of Substantially Equivalent on May 9, 2003. The device falls under product code LZU (Plug, Punctum), a Class U device. Lacrimedics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 2003
- Date Received
- January 29, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plug, Punctum
- Device Class
- Class U
- Regulation Number
- Review Panel
- OP
- Submission Type