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

SCANLAN VASCU-STATT II

K Number: K841515 · Decision Jun 5, 1984
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
5
Applicant Total
19
Review Days
54

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Basic Information

Device Name
SCANLAN VASCU-STATT II
K Number
K841515
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4070
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Scanlan Intl., Inc.
Date Received
April 12, 1984
Decision Date
June 5, 1984
Product Code
HRG
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HRG Engine, Trephine, Accessories, Ac-Powered

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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
K841514 SCANLAN VASCU-STATT II APPROXIMATOR
Search all 19 clearances from Scanlan Intl., Inc. →