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

NEONATAL CANNULA CAP

K Number: K864883 · Decision Jan 28, 1987
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
1
Review Days
47

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Basic Information

Device Name
NEONATAL CANNULA CAP
K Number
K864883
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Behan & Taylor Ent.
Date Received
December 12, 1986
Decision Date
January 28, 1987
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

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