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

AIRES TUOHY NEEDLES 17GA. X 4 1/2

K Number: K850111 · Decision Jan 24, 1985
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
19
Review Days
10

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
AIRES TUOHY NEEDLES 17GA. X 4 1/2
K Number
K850111
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Aries Medical, Inc.
Date Received
January 14, 1985
Decision Date
January 24, 1985
Product Code
BSP
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
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

Similar 510(k) Clearances

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

View all

Other Clearances by Aries Medical, Inc.

K Number Device Name
K912604 SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIF
K903925 ARIES MELDICAL MODEL 2100HC HANK CRANK
K903442 ARIES TAPERSEAL(TM) SHEATH
K895433 ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYS
K882289 ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.
K864994 40CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETER
K864537 40CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETER
K864568 40CC SURGICAL DOUBLE LUMEN BALLOON CATHETER
K864567 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
K871140 ARIES PEEL AWAY PERCUTANEOUS CATHETER INTRODUCER
Search all 19 clearances from Aries Medical, Inc. →