510(k) K801110
K801110 is an FDA 510(k) premarket notification submitted by American Optical Corp. for the device "PRESSURE MONITOR, MODEL 1131B". The FDA issued a decision of Substantially Equivalent on May 20, 1980. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. American Optical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 20, 1980
- Date Received
- May 12, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Computer, Blood-Pressure
- Device Class
- Class II
- Regulation Number
- 870.1110
- Review Panel
- CV
- Submission Type