510(k) K821932
K821932 is an FDA 510(k) premarket notification submitted by Mentor O & O, Inc. for the device "MENTOR POTENTIAL ACUITY METER". The FDA issued a decision of Substantially Equivalent on August 3, 1982. The device falls under product code HOX (Chart, Visual Acuity), a Class I device regulated under 21 CFR 886.1150. Mentor O & O, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 3, 1982
- Date Received
- June 29, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chart, Visual Acuity
- Device Class
- Class I
- Regulation Number
- 886.1150
- Review Panel
- OP
- Submission Type