510(k) K021055
K021055 is an FDA 510(k) premarket notification submitted by Busse Hospital Disposables, Inc. for the device "BUSSE UMBILICAL CORD CLAMP CUTTER". The FDA issued a decision of Substantially Equivalent on April 29, 2002. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530. Busse Hospital Disposables, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 29, 2002
- Date Received
- April 1, 2002
- 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