DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208
K-Number: K890298 · 1989-02-23
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Device Summary
Frequently Asked Questions
What is the DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208?
DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208 is a medical device that received FDA 510(k) clearance on 1989-02-23. The listed applicant is Salter Labs. The 510(k) number is K890298.
When did DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208 receive FDA 510(k) clearance?
DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208 received FDA 510(k) clearance on 1989-02-23, under 510(k) number K890298.
Who is the listed applicant for DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208?
The FDA 510(k) record lists Salter Labs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208?
The FDA product code for DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208 is NFB.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Salter Labs as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NFB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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