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FDA 510(k)

KEY MED FOREIGN BODY REMOVAL TUBE

K-Number: K813325 · 1982-02-10

ApplicantKeymed, Inc.
Decision Date1982-02-10
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEY MED FOREIGN BODY REMOVAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1982-02-10 under 510(k) number K813325. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEY MED FOREIGN BODY REMOVAL TUBE?

KEY MED FOREIGN BODY REMOVAL TUBE is a medical device that received FDA 510(k) clearance on 1982-02-10. The listed applicant is Keymed, Inc.. The 510(k) number is K813325.

When did KEY MED FOREIGN BODY REMOVAL TUBE receive FDA 510(k) clearance?

KEY MED FOREIGN BODY REMOVAL TUBE received FDA 510(k) clearance on 1982-02-10, under 510(k) number K813325.

Who is the listed applicant for KEY MED FOREIGN BODY REMOVAL TUBE?

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

What is the FDA product code for KEY MED FOREIGN BODY REMOVAL TUBE?

The FDA product code for KEY MED FOREIGN BODY REMOVAL TUBE is FED.

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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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