SCANLAN (TM) VEIN/GRAFT HOLDER— 510(k) K864919

Name: FDA 510(k) clearance K864919
Creator: U.S. Food and Drug Administration
Published: 1987-01-12

Substantially Equivalent

Scanlan Intl., Inc.

FDA 510(k) clearance K864919 for SCANLAN (TM) VEIN/GRAFT HOLDER, Substantially Equivalent on 1987-01-12. Applicant: Scanlan Intl., Inc.. Device class: 2.

Clearance details

Applicant: Scanlan Intl., Inc.
Product code: Code KPK
Device class: Class 2
Regulation: 21 CFR 878.4650
Advisory panel: General, Plastic Surgery
Date received: 1986-12-16
Decision date: 1987-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPK

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K971966 — CORONARY VEIN GRAFT TAG MARKER1998-01-26
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K864101 — COOK (R) VEIN GRAFT RING MARKERS1986-10-30
K801637 — FLUORO-MARK RADIOPAQUE ANATOMICAL MKR.1980-08-27
K770802 — MARKERS, STAINLESS STEEL1977-06-27

More clearances from Scanlan Intl., Inc.

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K960372 — SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM1996-04-26
K945474 — SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER1994-12-05
K911184 — SCANLAN/TAHERI VALVULOTOME1992-02-18
K864920 — SCANLAN (TM) INSTRUMENT TRAY1987-01-12
K851825 — SCANLAN TUNNELER, SHEATH & TIP1985-07-12

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