510(k) K873919
K873919 is an FDA 510(k) premarket notification submitted by Richmond Products, Inc. for the device "TANGENT SCREEN". The FDA issued a decision of Substantially Equivalent on October 28, 1987. The device falls under product code HOJ (Screen, Tangent, Target), a Class I device regulated under 21 CFR 886.1810. Richmond Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1987
- Date Received
- September 25, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screen, Tangent, Target
- Device Class
- Class I
- Regulation Number
- 886.1810
- Review Panel
- OP
- Submission Type