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

SCANLAN TUNNELER, SHEATH & TIP

K Number: K851825 · Decision Jul 12, 1985
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
19
Review Days
77

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Basic Information

Device Name
SCANLAN TUNNELER, SHEATH & TIP
K Number
K851825
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Scanlan Intl., Inc.
Date Received
April 26, 1985
Decision Date
July 12, 1985
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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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
K841521 SCANLAN ENDARSECTOR
K841513 SCANLAN ATRAUM INSTRUMENT JAW COVER
K841085 SCANLAN COLORMARK SKIN MARKER
K841515 SCANLAN VASCU-STATT II
K841514 SCANLAN VASCU-STATT II APPROXIMATOR
Search all 19 clearances from Scanlan Intl., Inc. →