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

QUICK-LOCK

K Number: K945816 · Decision Jan 13, 1995
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
23
Review Days
46

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Basic Information

Device Name
QUICK-LOCK
K Number
K945816
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
B&B Medical Technologies, Inc.
Date Received
November 28, 1994
Decision Date
January 13, 1995
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

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Other Clearances by B&B Medical Technologies, Inc.

K Number Device Name
K030396 OMNI~NEB; OMNI~MAX
K980407 HOPE NEBULIZER
K960663 UNIVERSAL BITE BLOCK
K944324 SURE-LOCK VENTILATOR TUBING HOLDER
K935171 STABILTRACH
K925386 ADHESIVE E.T. TAPE
K923690 MINI HEART
K913015 HEART NEBULIZER FLOWMETER ADAPTOR
K913753 BODAI NEO2 -SAFE AIRWAY PRESSURE CAP
K913000 HEART NEBULIZER POLE CLAMP
Search all 23 clearances from B&B Medical Technologies, Inc. →