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

NEEDLE DRIVER

K Number: K780255 · Decision Apr 18, 1978
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
1
Applicant Total
19
Review Days
61

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Basic Information

Device Name
NEEDLE DRIVER
K Number
K780255
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Scanlan Intl., Inc.
Date Received
February 16, 1978
Decision Date
April 18, 1978
Product Code
GFC
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
GFC Driver, Surgical, Pin

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Other Clearances by Scanlan Intl., Inc.

K Number Device Name
K960372 SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM
K945474 SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER
K911184 SCANLAN/TAHERI VALVULOTOME
K864920 SCANLAN (TM) INSTRUMENT TRAY
K864919 SCANLAN (TM) VEIN/GRAFT HOLDER
K851825 SCANLAN TUNNELER, SHEATH & TIP
K841521 SCANLAN ENDARSECTOR
K841513 SCANLAN ATRAUM INSTRUMENT JAW COVER
K841085 SCANLAN COLORMARK SKIN MARKER
K841515 SCANLAN VASCU-STATT II
Search all 19 clearances from Scanlan Intl., Inc. →