FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FRANZEN NEEDLE GUIDE

K Number: K830235 · Decision Feb 23, 1983
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
25
Review Days
29

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Basic Information

Device Name
FRANZEN NEEDLE GUIDE
K Number
K830235
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Precision Dynamics Corp.
Date Received
January 25, 1983
Decision Date
February 23, 1983
Product Code
GDM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDM Needle, Aspiration And Injection, Reusable

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Other Clearances by Precision Dynamics Corp.

K Number Device Name
K020718 SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
K994353 SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565
K994263 SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
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
Search all 25 clearances from Precision Dynamics Corp. →