510(k) K800722
K800722 is an FDA 510(k) premarket notification submitted by Cavitron Corp. for the device "AUTO-FIELD D AUTOMATED VISUAL DETECTOR". The FDA issued a decision of Substantially Equivalent on April 29, 1980. The device falls under product code HPT (Perimeter, Automatic, Ac-Powered), a Class I device regulated under 21 CFR 886.1605. Cavitron Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 29, 1980
- Date Received
- April 1, 1980
- 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