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

CPAP INFANT NASAL CANNULAE SET

K Number: K823936 · Decision Jan 28, 1983
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
42
Review Days
30

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Basic Information

Device Name
CPAP INFANT NASAL CANNULAE SET
K Number
K823936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Ackrad Laboratories
Date Received
December 29, 1982
Decision Date
January 28, 1983
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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Other Clearances by Ackrad Laboratories

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K020951 H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007
K970492 INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
K961752 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
K940176 ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION
K952542 ACKRAD ESOPHAGEAL BALLOON CATHETER SET
K953034 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
K915813 ACKRAD ERCP CONTRAST DELIVERY SET
K904499 NICOS (NON-INVASIVE CARDIAC OUTPUT SYSTEM)
Search all 42 clearances from Ackrad Laboratories →