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FDA 510(k)

WILLIAMS OESOPHAGEAL VARICES INJECT TUBE

K-Number: K810180 · 1981-02-09

ApplicantKeymed, Inc.
Decision Date1981-02-09
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILLIAMS OESOPHAGEAL VARICES INJECT 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 1981-02-09 under 510(k) number K810180. 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 WILLIAMS OESOPHAGEAL VARICES INJECT TUBE?

WILLIAMS OESOPHAGEAL VARICES INJECT TUBE is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Keymed, Inc.. The 510(k) number is K810180.

When did WILLIAMS OESOPHAGEAL VARICES INJECT TUBE receive FDA 510(k) clearance?

WILLIAMS OESOPHAGEAL VARICES INJECT TUBE received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810180.

Who is the listed applicant for WILLIAMS OESOPHAGEAL VARICES INJECT 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 WILLIAMS OESOPHAGEAL VARICES INJECT TUBE?

The FDA product code for WILLIAMS OESOPHAGEAL VARICES INJECT 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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