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

ARROW POSITIVE PLACEMENT CON/EPIDURAL AN

K Number: K801912 · Decision Sep 16, 1980
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
110
Review Days
36

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 POSITIVE PLACEMENT CON/EPIDURAL AN
K Number
K801912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Arrow Intl., Inc.
Date Received
August 11, 1980
Decision Date
September 16, 1980
Product Code
CAZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAZ Anesthesia Conduction Kit

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAZ), 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
K071491 ARROW INTERNATIONAL, INC., SURGICAL DRAPES
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
Search all 110 clearances from Arrow Intl., Inc. →