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

BLOCK, BITE, INTUBATION

K Number: K873491 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
18
Applicant Total
23
Review Days
50

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Basic Information

Device Name
BLOCK, BITE, INTUBATION
K Number
K873491
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5280
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
B&B Medical Technologies, Inc.
Date Received
August 31, 1987
Decision Date
October 20, 1987
Product Code
JAY
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
JAY Support, Breathing Tube

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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
K945816 QUICK-LOCK
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
Search all 23 clearances from B&B Medical Technologies, Inc. →