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FDA 510(k)

CANNULA, DISPOSABLE OXYGEN TTHERAPY

K-Number: K760330 · 1976-08-04

Decision Date1976-08-04
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CANNULA, DISPOSABLE OXYGEN TTHERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Inhal-O-Tech Medical Plastic. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760330. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA, DISPOSABLE OXYGEN TTHERAPY?

CANNULA, DISPOSABLE OXYGEN TTHERAPY is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Inhal-O-Tech Medical Plastic. The 510(k) number is K760330.

When did CANNULA, DISPOSABLE OXYGEN TTHERAPY receive FDA 510(k) clearance?

CANNULA, DISPOSABLE OXYGEN TTHERAPY received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760330.

Who is the listed applicant for CANNULA, DISPOSABLE OXYGEN TTHERAPY?

The FDA 510(k) record lists Inhal-O-Tech Medical Plastic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANNULA, DISPOSABLE OXYGEN TTHERAPY?

The FDA product code for CANNULA, DISPOSABLE OXYGEN TTHERAPY 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 Inhal-O-Tech Medical Plastic 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.

View all 7 devices →

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

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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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