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FDA 510(k)

ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330

K-Number: K780812 · 1978-06-13

ApplicantHoneywell, Inc.
Decision Date1978-06-13
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1978-06-13 under 510(k) number K780812. 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 SYSTEM - MODEL 3330?

ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330 is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Honeywell, Inc.. The 510(k) number is K780812.

When did ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330 receive FDA 510(k) clearance?

ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330 received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780812.

Who is the listed applicant for ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330?

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 SYSTEM - MODEL 3330?

The FDA product code for ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330 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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