510(k) K896175
K896175 is an FDA 510(k) premarket notification submitted by Lacrimedics, Inc. for the device "HERRICK LACRIMAL PLUG TM.". The FDA issued a decision of Substantially Equivalent on January 22, 1990. 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
- January 22, 1990
- Date Received
- October 25, 1989
- 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