LIGHTWEIGHT PLASTIC CANNULA
K-Number: K770487 · 1977-03-21
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Device Summary
Frequently Asked Questions
What is the LIGHTWEIGHT PLASTIC CANNULA?
LIGHTWEIGHT PLASTIC CANNULA is a medical device that received FDA 510(k) clearance on 1977-03-21. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K770487.
When did LIGHTWEIGHT PLASTIC CANNULA receive FDA 510(k) clearance?
LIGHTWEIGHT PLASTIC CANNULA received FDA 510(k) clearance on 1977-03-21, under 510(k) number K770487.
Who is the listed applicant for LIGHTWEIGHT PLASTIC CANNULA?
The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGHTWEIGHT PLASTIC CANNULA?
The FDA product code for LIGHTWEIGHT PLASTIC CANNULA is CAT.
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 Hudson Oxygen Therapy Sales Co. 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: CAT)
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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