510(k) K971242
K971242 is an FDA 510(k) premarket notification submitted by Ipax, Inc. for the device "BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28)". The FDA issued a decision of Substantially Equivalent on December 17, 1997. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700. Ipax, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 17, 1997
- Date Received
- April 2, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Weights, Eyelid, External
- Device Class
- Class II
- Regulation Number
- 886.5700
- Review Panel
- OP
- Submission Type
Gravity assisted treatment of lagophthalmos (incomplete eyelid closure)