510(k) K852639
K852639 is an FDA 510(k) premarket notification submitted by Zeiss Humphrey System for the device "HUMPHREY FIELD ANALYZER MODEL 630". The FDA issued a decision of Substantially Equivalent on September 18, 1985. The device falls under product code HPT (Perimeter, Automatic, Ac-Powered), a Class I device regulated under 21 CFR 886.1605. Zeiss Humphrey System has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 18, 1985
- Date Received
- June 20, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Perimeter, Automatic, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 886.1605
- Review Panel
- OP
- Submission Type