510(k) K020718

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE by Precision Dynamics Corp. — Product Code HFW

K020718 is an FDA 510(k) premarket notification submitted by Precision Dynamics Corp. for the device "SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE". The FDA issued a decision of Substantially Equivalent on June 3, 2002. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530. Precision Dynamics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 2002
Date Received
March 5, 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