HBO-1 PASS-THROUGH/EXTENSION TUBE
K-Number: K832434 · 1983-09-20
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Device Summary
Frequently Asked Questions
What is the HBO-1 PASS-THROUGH/EXTENSION TUBE?
HBO-1 PASS-THROUGH/EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1983-09-20. The listed applicant is Nauset Labs. The 510(k) number is K832434.
When did HBO-1 PASS-THROUGH/EXTENSION TUBE receive FDA 510(k) clearance?
HBO-1 PASS-THROUGH/EXTENSION TUBE received FDA 510(k) clearance on 1983-09-20, under 510(k) number K832434.
Who is the listed applicant for HBO-1 PASS-THROUGH/EXTENSION TUBE?
The FDA 510(k) record lists Nauset Labs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HBO-1 PASS-THROUGH/EXTENSION TUBE?
The FDA product code for HBO-1 PASS-THROUGH/EXTENSION TUBE is FPA.
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.
Related Devices (Code: FPA)
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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