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

SPINAL TAP NEEDLE

K Number: K910652 · Decision Jul 24, 1991
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
26
Review Days
160

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Basic Information

Device Name
SPINAL TAP NEEDLE
K Number
K910652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Gesco Intl., Inc.
Date Received
February 14, 1991
Decision Date
July 24, 1991
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

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Other Clearances by Gesco Intl., Inc.

K Number Device Name
K954422 PER-Q-CATH MID-LINE
K940953 UMBILI-CATH-S
K940870 UMBILI-CATH
K940952 UMBILI-CATH-S-DL
K941672 URI-CATH CATHETER
K941232 THORA-CATH
K940871 UMBILI-CATH-P
K931989 VENTRI-CATH
K926063 PER-Q-CATH DRESSING CHANGE TRAY
K923591 PALA-NATE
Search all 26 clearances from Gesco Intl., Inc. →