510(k) K945841
K945841 is an FDA 510(k) premarket notification submitted by W G M Corp. for the device "BIRTH THEFT INFANT IDENTIFICATION AND PROTECTION UMBILICAL CORD CLAMP". The FDA issued a decision of Substantially Equivalent on May 30, 1995. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 1995
- Date Received
- November 30, 1994
- 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