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

SALTER LABS DISPOSABLE NIPPLE AND NUT

K Number: K912174 · Decision Jul 24, 1991
Classifications
1
FEI Numbers
111
Registration Numbers
112
Same Product Code
54
Applicant Total
48
Review Days
69

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Basic Information

Device Name
SALTER LABS DISPOSABLE NIPPLE AND NUT
K Number
K912174
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.2700
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Salter Labs
Date Received
May 16, 1991
Decision Date
July 24, 1991
Product Code
CAN
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
CAN Regulator, Pressure, Gas Cylinder

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K151506 Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula
K151421 Nasal CO2 Sample Line, Oral Nasal CO2 Sampling Cannula, O2 Oral/Nasal Co2 Cannula, Sample Lines
K143700 CPAP Cannulaide
K142416 Luma Wrap
K092685 PNEUMOTHERML, MODEL: 5800
K051313 BI-NAPS NASAL AIRFLOW AND SNORE TRANSDUCER
K040202 SALTER LABS CPAP HIGH FLOW CANNULA SYSTEM
K014056 SALTER LABS MODIFIED NEBUTECH NEBULIZER
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