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FDA 510(k)

ESOPHAGEAL MOTILITY TUBE

K-Number: K760761 · 1976-11-30

ApplicantSherwood Medical Industries
Decision Date1976-11-30
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL MOTILITY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-11-30 under 510(k) number K760761. 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 TUBE?

ESOPHAGEAL MOTILITY TUBE is a medical device that received FDA 510(k) clearance on 1976-11-30. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760761.

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

ESOPHAGEAL MOTILITY TUBE received FDA 510(k) clearance on 1976-11-30, under 510(k) number K760761.

Who is the listed applicant for ESOPHAGEAL MOTILITY TUBE?

The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESOPHAGEAL MOTILITY TUBE?

The FDA product code for ESOPHAGEAL MOTILITY TUBE is FFX.

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Other records listing Sherwood Medical Industries as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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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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