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

SECURLINE SURGICAL SKIN MARKER 1000

K Number: K840820 · Decision Apr 25, 1984
Classifications
1
FEI Numbers
183
Registration Numbers
184
Same Product Code
22
Applicant Total
25
Review Days
61

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Basic Information

Device Name
SECURLINE SURGICAL SKIN MARKER 1000
K Number
K840820
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4660
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Precision Dynamics Corp.
Date Received
February 24, 1984
Decision Date
April 25, 1984
Product Code
FZZ
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
FZZ Marker, Skin

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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. →