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FDA 510(k)

HBO-1 PASS-THROUGH/EXTENSION TUBE

K-Number: K832434 · 1983-09-20

ApplicantNauset Labs
Decision Date1983-09-20
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HBO-1 PASS-THROUGH/EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Nauset Labs. It received FDA 510(k) clearance on 1983-09-20 under 510(k) number K832434. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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