510(k) K944585
K944585 is an FDA 510(k) premarket notification submitted by Prentke Romich Co. for the device "SCANNING DIRECTOR". The FDA issued a decision of Substantially Equivalent on February 21, 1995. The device falls under product code IQA (System, Environmental Control, Powered), a Class II device regulated under 21 CFR 890.3725. Prentke Romich Co. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 21, 1995
- Date Received
- September 19, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Environmental Control, Powered
- Device Class
- Class II
- Regulation Number
- 890.3725
- Review Panel
- PM
- Submission Type