510(k) K860904
K860904 is an FDA 510(k) premarket notification submitted by Medline Industries, Inc. for the device "VIDEO PRINTER, MODEL 3200". The FDA issued a decision of Substantially Equivalent on March 28, 1986. The device falls under product code KQM (Camera, Surgical And Accessories), a Class I device regulated under 21 CFR 878.4160. Medline Industries, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 28, 1986
- Date Received
- March 10, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Camera, Surgical And Accessories
- Device Class
- Class I
- Regulation Number
- 878.4160
- Review Panel
- SU
- Submission Type