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FDA 510(k)

VENTILATION TUBES WITH HYDROGEL COATING

K-Number: K870129 · 1987-02-10

Decision Date1987-02-10
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VENTILATION TUBES WITH HYDROGEL COATING is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870129. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTILATION TUBES WITH HYDROGEL COATING?

VENTILATION TUBES WITH HYDROGEL COATING is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K870129.

When did VENTILATION TUBES WITH HYDROGEL COATING receive FDA 510(k) clearance?

VENTILATION TUBES WITH HYDROGEL COATING received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870129.

Who is the listed applicant for VENTILATION TUBES WITH HYDROGEL COATING?

The FDA 510(k) record lists Richards Medical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTILATION TUBES WITH HYDROGEL COATING?

The FDA product code for VENTILATION TUBES WITH HYDROGEL COATING is ETD.

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 Richards Medical Co., Inc. 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 71 devices →

Related Devices (Code: ETD)

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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