SCANLAN VASCU-STATT— 510(k) K802829

Substantially Equivalent

Scanlan Intl., Inc.

FDA 510(k) clearance K802829 for SCANLAN VASCU-STATT, Substantially Equivalent on 1981-01-15. Applicant: Scanlan Intl., Inc.. Device class: 1.

Clearance details

Applicant: Scanlan Intl., Inc.
Product code: Code FMP
Device class: Class 1
Regulation: 21 CFR 880.6450
Advisory panel: General Hospital
Date received: 1980-11-10
Decision date: 1981-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FMP

K150243 — Invictus Medical GelShield2015-05-01
K951325 — COMFEEL PLUS PRESSURE RELIEF DRESSING1995-07-31
K934731 — MEDSURG STERILE IMAGING PRODUCTS1994-03-28
K820584 — DECUBICARE PADS & ACCESSORIES1982-03-25
K812344 — HEEL OR ELBOW PROTECTOR1981-09-11

More clearances from Scanlan Intl., Inc.

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
K864919 — SCANLAN (TM) VEIN/GRAFT HOLDER1987-01-12
K864920 — SCANLAN (TM) INSTRUMENT TRAY1987-01-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.