510(k) K863040
K863040 is an FDA 510(k) premarket notification submitted by Cher Mel Corp. for the device "DISPOSABLE INTRAVENOUS HYPERALIMENTATION BAGS". The FDA issued a decision of Substantially Equivalent on October 31, 1986. The device falls under product code KPE (Container, I.V.), a Class II device regulated under 21 CFR 880.5025. Cher Mel Corp. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 1986
- Date Received
- August 12, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Container, I.V.
- Device Class
- Class II
- Regulation Number
- 880.5025
- Review Panel
- HO
- Submission Type