510(k) K943463
K943463 is an FDA 510(k) premarket notification submitted by Intl. Remote Imaging Systems for the device "THE YELLOW IRIS". The FDA issued a decision of Substantially Equivalent on September 20, 1994. The device falls under product code KQO (Automated Urinalysis System), a Class I device regulated under 21 CFR 862.2900. Intl. Remote Imaging Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 20, 1994
- Date Received
- July 18, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Automated Urinalysis System
- Device Class
- Class I
- Regulation Number
- 862.2900
- Review Panel
- CH
- Submission Type