510(k) K923127
K923127 is an FDA 510(k) premarket notification submitted by Concord/Portex for the device "NEEDLE-PRO CARTRIDGE". The FDA issued a decision of Substantially Equivalent on April 29, 1993. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Concord/Portex has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 29, 1993
- Date Received
- June 26, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Hypodermic, Single Lumen
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type