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FDA 510(k)

REUTER BOBBIN VENTILA. TUBE-TITANIUM

K-Number: K820362 · 1982-03-02

ApplicantRichard'S Medical Equip., Inc.
Decision Date1982-03-02
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

REUTER BOBBIN VENTILA. TUBE-TITANIUM is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1982-03-02 under 510(k) number K820362. 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 REUTER BOBBIN VENTILA. TUBE-TITANIUM?

REUTER BOBBIN VENTILA. TUBE-TITANIUM is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K820362.

When did REUTER BOBBIN VENTILA. TUBE-TITANIUM receive FDA 510(k) clearance?

REUTER BOBBIN VENTILA. TUBE-TITANIUM received FDA 510(k) clearance on 1982-03-02, under 510(k) number K820362.

Who is the listed applicant for REUTER BOBBIN VENTILA. TUBE-TITANIUM?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REUTER BOBBIN VENTILA. TUBE-TITANIUM?

The FDA product code for REUTER BOBBIN VENTILA. TUBE-TITANIUM is ETD.

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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.

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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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