FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE

K Number: K020718 · Decision Jun 3, 2002
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
35
Applicant Total
25
Review Days
90

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Basic Information

Device Name
SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
K Number
K020718
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precision Dynamics Corp.
Date Received
March 5, 2002
Decision Date
June 3, 2002
Product Code
HFW
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HFW Clamp, Umbilical

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Other Clearances by Precision Dynamics Corp.

K Number Device Name
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K990737 'ECURLINE UMBILICAL CORD CLAMP #3500
K884357 PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM
K882580 MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE
K874665 SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
K873369 SECURLINE FRANSEENE NEEDLE
K872507 PRECISION CULTURE C.A.T.S. COLLECT/TRANS HSV I/II
K863164 AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA
K851364 FRANZEN NEEDLE GUIDE FOR TRANSRECTAL PROSTATE BIOP
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