FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ABG POINT LOK NEEDLE PROTECTION DEVICE

K Number: K954015 · Decision Nov 20, 1995
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
57
Applicant Total
47
Review Days
87

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Basic Information

Device Name
ABG POINT LOK NEEDLE PROTECTION DEVICE
K Number
K954015
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1100
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Devon Industries, Inc.
Date Received
August 25, 1995
Decision Date
November 20, 1995
Product Code
CBT
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
CBT Arterial Blood Sampling Kit

Similar 510(k) Clearances

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

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Other Clearances by Devon Industries, Inc.

K Number Device Name
K961993 BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)
K946289 DEVONS POINT LOK NEEDLE PROTECTION DEVICE
K945197 THE SHARPS COLLECTION AND DISPOSAL SYSTEM
K943892 POINT OF USE SHARPS A GATOR
K944114 PHLEBOTOMY UNIT SHARPS A GATOR
K945485 ABG NEEDLE PROTECTION
K932998 EASY-ON
K912824 DEVON SPONGE COUNTER BAGS
K894170 DEVON DISPOSABLE HEAD POSITIONER COVER
K892660 HIBERNATION KIT
Search all 47 clearances from Devon Industries, Inc. →