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FDA 510(k)

ESOPHAGEAL MOTILITY APPARATUS

K-Number: K812103 · 1981-08-13

ApplicantHoneywell, Inc.
Decision Date1981-08-13
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL MOTILITY APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K812103. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL MOTILITY APPARATUS?

ESOPHAGEAL MOTILITY APPARATUS is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Honeywell, Inc.. The 510(k) number is K812103.

When did ESOPHAGEAL MOTILITY APPARATUS receive FDA 510(k) clearance?

ESOPHAGEAL MOTILITY APPARATUS received FDA 510(k) clearance on 1981-08-13, under 510(k) number K812103.

Who is the listed applicant for ESOPHAGEAL MOTILITY APPARATUS?

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

What is the FDA product code for ESOPHAGEAL MOTILITY APPARATUS?

The FDA product code for ESOPHAGEAL MOTILITY APPARATUS is FFX.

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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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