510(k) K862519
K862519 is an FDA 510(k) premarket notification submitted by Bausch & Lomb, Inc. for the device "BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR". The FDA issued a decision of Substantially Equivalent on July 23, 1986. The device falls under product code HOS (Projector, Ophthalmic), a Class I device regulated under 21 CFR 886.1680. Bausch & Lomb, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 23, 1986
- Date Received
- July 1, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Projector, Ophthalmic
- Device Class
- Class I
- Regulation Number
- 886.1680
- Review Panel
- OP
- Submission Type