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

CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCK

K Number: K993619 · Decision Apr 28, 2000
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
12
Review Days
185

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Basic Information

Device Name
CSECURE COMBINED SPINAL/EPIDURAL ANESTHESIA SYSTEM WITH LOCK
K Number
K993619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sims Portex, Inc.
Date Received
October 26, 1999
Decision Date
April 28, 2000
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.

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Other Clearances by Sims Portex, Inc.

K Number Device Name
K011925 HYPODERMIC NEEDLE-PRO NEEDLE WITH NEEDLE PROTECTION DEVICE; HYPODERMIC NEEDLE-PRO SYRINGE & NEEDLE WITH NEEDLE PROTECTIO
K002201 ELECTROSTATIC HYDROPHOBIC BREATHING FILTER
K002506 BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT
K001318 CPAP SYSTEM, MODEL 102001
K994275 SIMS PORTEX ANESTHESIA CATHETER
K991861 1ST RESPONSE INFANT MANUAL RESUSCITATOR, BAG RESEVOIR, 1ST RESPONSE PEDIATRIC MANUAL RESUSCITATOR, BAG RESERVOIR, 1ST RE
K992471 SIMS PORTEX EPIDURAL CATHETER, 20G MODEL# 4910-16/17; 21G MODEL# 4910-18
K992057 IST RESPONSE MANUAL RESUSCITATOR, MODELS, 008000, 008003,008006
K983858 SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES
K981035 PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES
Search all 12 clearances from Sims Portex, Inc. →