510(k) K872729
K872729 is an FDA 510(k) premarket notification submitted by Camtec for the device "INFUSION STAND". The FDA issued a decision of Substantially Equivalent on July 23, 1987. The device falls under product code FOX (Stand, Infusion), a Class I device regulated under 21 CFR 880.6990. Camtec has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 23, 1987
- Date Received
- July 8, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stand, Infusion
- Device Class
- Class I
- Regulation Number
- 880.6990
- Review Panel
- HO
- Submission Type