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FDA 510(k)

BIO-VENT REUTER BOBBIN TUBE

K-Number: K870877 · 1987-03-26

ApplicantRichards Medical Co., Inc.
Decision Date1987-03-26
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BIO-VENT REUTER BOBBIN TUBE 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 1987-03-26 under 510(k) number K870877. 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 BIO-VENT REUTER BOBBIN TUBE?

BIO-VENT REUTER BOBBIN TUBE is a medical device that received FDA 510(k) clearance on 1987-03-26. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K870877.

When did BIO-VENT REUTER BOBBIN TUBE receive FDA 510(k) clearance?

BIO-VENT REUTER BOBBIN TUBE received FDA 510(k) clearance on 1987-03-26, under 510(k) number K870877.

Who is the listed applicant for BIO-VENT REUTER BOBBIN TUBE?

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 BIO-VENT REUTER BOBBIN TUBE?

The FDA product code for BIO-VENT REUTER BOBBIN TUBE is ETD.

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Other records listing Richards Medical Co., Inc. as applicant

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Related Devices (Code: ETD)

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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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