FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARROW INTERNATIONAL, INC., SURGICAL DRAPES

K Number: K071491 · Decision Oct 10, 2007
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
110
Review Days
133

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARROW INTERNATIONAL, INC., SURGICAL DRAPES
K Number
K071491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arrow Intl., Inc.
Date Received
May 30, 2007
Decision Date
October 10, 2007
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KKX), ordered by most recent decision date.

View all

Other Clearances by Arrow Intl., Inc.

K Number Device Name
K100635 ARROWGARD EVOLUTION ANTIMICROBIAL PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) MODEL: S-44041-002, S-45041-002, S-45504
K093050 ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520
K071998 ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT
K071111 NON-ABSORBABLE SILK SUTURE
K060309 AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES
K042126 PICC
K041153 SHARPSAWAY II LOCKING DISPOSABLE CUP
K040801 INTRA-AORTIC BALLOON (IAB)
K040802 HEMOSONIC 200HEMODYNAMIC MONITOR
K040100 ARROW ECHOGENIC INTRODUCER NEEDLE
Search all 110 clearances from Arrow Intl., Inc. →