510(k) K012917
K012917 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B". The FDA issued a decision of Substantially Equivalent on November 28, 2001. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530. Dynarex Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 28, 2001
- Date Received
- August 30, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clamp, Umbilical
- Device Class
- Class II
- Regulation Number
- 884.4530
- Review Panel
- OB
- Submission Type